Canonical Allele Identifier: CA1689218256
Gene:

Linked Data

dbSNP Id: rs1379079347

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400681A>G , CM000669.2:g.13400681A>G GRCh38
NC_000007.13:g.13440306A>G , CM000669.1:g.13440306A>G GRCh37
NC_000007.12:g.13406831A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745097.1:n.147+90358A>G