Canonical Allele Identifier: CA55353845
Gene:

Linked Data

dbSNP Id: rs1021386907

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431662C>T , CM000664.2:g.127431662C>T GRCh38
NC_000002.11:g.128189238C>T , CM000664.1:g.128189238C>T GRCh37
NC_000002.10:g.127905708C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1331+5G>A
XR_001739705.1:n.3607-3398G>A
XR_923313.2:n.4042+5G>A