Canonical Allele Identifier: CA2485976197
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682242A= , CM000663.2:g.213682242A= GRCh38
NC_000001.10:g.213855585A= , CM000663.1:g.213855585A= GRCh37
NC_000001.9:g.211922208A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738463.1:n.601-49175A=
XR_001738464.1:n.426-49175A=