Canonical Allele Identifier: CA1258276528
Gene:

Linked Data

dbSNP Id: rs1558645454

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.67637488T>C , CM000664.2:g.67637488T>C GRCh38
NC_000002.11:g.67864620T>C , CM000664.1:g.67864620T>C GRCh37
NC_000002.10:g.67718124T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739524.1:n.65+13478A>G