Canonical Allele Identifier: CA1181643459
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94587878A= , CM000663.2:g.94587878A= GRCh38
NC_000001.10:g.95053434A= , CM000663.1:g.95053434A= GRCh37
NC_000001.9:g.94826022A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738161.1:n.461+24265A=