Canonical Allele Identifier: CA1985859969
Gene:

Linked Data

dbSNP Id: rs1857709822

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851733G>A , CM000673.2:g.80851733G>A GRCh38
NC_000011.9:g.80562776G>A , CM000673.1:g.80562776G>A GRCh37
NC_000011.8:g.80240424G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.124+60558C>T