Canonical Allele Identifier: CA1140461318
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94587871G= , CM000663.2:g.94587871G= GRCh38
NC_000001.10:g.95053427G= , CM000663.1:g.95053427G= GRCh37
NC_000001.9:g.94826015G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+24258G=