Canonical Allele Identifier: CA1224246998
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224887063G= , CM000663.2:g.224887063G= GRCh38
NC_000001.10:g.225074765G= , CM000663.1:g.225074765G= GRCh37
NC_000001.9:g.223141388G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949207.1:n.66-2282C=
XR_949207.2:n.63-2282C=