Canonical Allele Identifier: CA756632623
Gene:

Linked Data

dbSNP Id: rs1318487034

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431634G>C , CM000664.2:g.127431634G>C GRCh38
NC_000002.11:g.128189210G>C , CM000664.1:g.128189210G>C GRCh37
NC_000002.10:g.127905680G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1331+33C>G
XR_001739705.1:n.3607-3370C>G
XR_923313.2:n.4042+33C>G