Canonical Allele Identifier: CA1009193448
Gene:

Linked Data

dbSNP Id: rs1660426616

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741892G>T , CM000663.2:g.172741892G>T GRCh38
NC_000001.10:g.172711032G>T , CM000663.1:g.172711032G>T GRCh37
NC_000001.9:g.170977655G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-33927G>T