Canonical Allele Identifier: CA626487385
Gene:

Linked Data

dbSNP Id: rs1284792261

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211750T>G , CM000679.2:g.50211750T>G GRCh38
NC_000017.10:g.48289111T>G , CM000679.1:g.48289111T>G GRCh37
NC_000017.9:g.45644110T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-2085T>G