Canonical Allele Identifier: CA1218511494
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.198500009T= , CM000663.2:g.198500009T= GRCh38
NC_000001.10:g.198469139T= , CM000663.1:g.198469139T= GRCh37
NC_000001.9:g.196735762T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922398.1:n.679+19542A=
XR_922398.2:n.341+19542A=