ClinVar

NM_001770.6(CD19):c.1383T>C (p.Tyr461=)

Gene:

CD19:CD19 molecule [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16p11.2

Genomic location:

• Chr16: 28937634 (on Assembly GRCh38)
• Chr16: 28948955 (on Assembly GRCh37)

Preferred name:

NM_001770.6(CD19):c.1383T>C (p.Tyr461=)

HGVS:

• NC_000016.10:g.28937634T>C
• NG_007275.1:g.10696T>C
• NM_001178098.2:c.1383T>C
• NM_001385732.1:c.1116T>C
• NM_001770.6:c.1383T>CMANE SELECT
• NP_001171569.1:p.Tyr461=
• NP_001372661.1:p.Tyr372=
• NP_001761.3:p.Tyr461=
• LRG_35:g.10696T>C
• NC_000016.9:g.28948955T>C
• NR_169755.1:n.1725T>C

This HGVS expression did not pass validation

Links:

dbSNP: rs1964807778

NCBI 1000 Genomes Browser:

rs1964807778

Molecular consequence:

• NR_169755.1:n.1725T>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_001178098.2:c.1383T>C - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001385732.1:c.1116T>C - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001770.6:c.1383T>C - synonymous variant - [Sequence Ontology: SO:0001819]