Canonical Allele Identifier: CA1223909896
Gene:

Linked Data

dbSNP Id: rs1655906794

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068548G>A , CM000663.2:g.224068548G>A GRCh38
NC_000001.10:g.224256250G>A , CM000663.1:g.224256250G>A GRCh37
NC_000001.9:g.222322873G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+894G>A
XR_001737824.1:n.242+894G>A