Canonical Allele Identifier: CA1036161579
Gene:

Linked Data

dbSNP Id: rs1688786682

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431682G>A , CM000664.2:g.127431682G>A GRCh38
NC_000002.11:g.128189258G>A , CM000664.1:g.128189258G>A GRCh37
NC_000002.10:g.127905728G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1316C>T
XR_001739705.1:n.3607-3418C>T
XR_923313.2:n.4027C>T