Canonical Allele Identifier: CA1140106548
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224887034T= , CM000663.2:g.224887034T= GRCh38
NC_000001.10:g.225074736T= , CM000663.1:g.225074736T= GRCh37
NC_000001.9:g.223141359T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949207.1:n.66-2253A=
XR_949207.2:n.63-2253A=