Canonical Allele Identifier: CA55353802
Gene:

Linked Data

dbSNP Id: rs1049220443

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431639G>A , CM000664.2:g.127431639G>A GRCh38
NC_000002.11:g.128189215G>A , CM000664.1:g.128189215G>A GRCh37
NC_000002.10:g.127905685G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1331+28C>T
XR_001739705.1:n.3607-3375C>T
XR_923313.2:n.4042+28C>T