Canonical Allele Identifier: CA1740470166
Gene:

Linked Data

dbSNP Id: rs1795647213

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306449T>G , CM000669.2:g.124306449T>G GRCh38
NC_000007.13:g.123946503T>G , CM000669.1:g.123946503T>G GRCh37
NC_000007.12:g.123733739T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956584.1:n.73-29T>G