Canonical Allele Identifier: CA1286885919
Gene:

Linked Data

dbSNP Id: rs1688785332

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431598A>T , CM000664.2:g.127431598A>T GRCh38
NC_000002.11:g.128189174A>T , CM000664.1:g.128189174A>T GRCh37
NC_000002.10:g.127905644A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1331+69T>A
XR_001739705.1:n.3607-3334T>A
XR_923313.2:n.4042+69T>A