Canonical Allele Identifier: CA1728106780
Gene:

Linked Data

dbSNP Id: rs1789258494

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388599A>G , CM000669.2:g.97388599A>G GRCh38
NC_000007.13:g.97017911A>G , CM000669.1:g.97017911A>G GRCh37
NC_000007.12:g.96855847A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59952T>C