Canonical Allele Identifier: CA2397855721
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573086C= , CM000684.2:g.23573086C= GRCh38
NC_000022.10:g.23915273C= , CM000684.1:g.23915273C= GRCh37
NC_000022.9:g.22245273C= NCBI36
NG_009791.1:g.12223G= , LRG_69:g.12223G=

Transcript Alleles

HGVS Amino-acid Change
XR_938078.1:n.691C=
XR_938078.2:n.1275C=