Canonical Allele Identifier: CA1223909919
Gene:

Linked Data

dbSNP Id: rs1655907350

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068622G>A , CM000663.2:g.224068622G>A GRCh38
NC_000001.10:g.224256324G>A , CM000663.1:g.224256324G>A GRCh37
NC_000001.9:g.222322947G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+968G>A
XR_001737824.1:n.242+968G>A