Canonical Allele Identifier: CA2397855716
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573071C= , CM000684.2:g.23573071C= GRCh38
NC_000022.10:g.23915258C= , CM000684.1:g.23915258C= GRCh37
NC_000022.9:g.22245258C= NCBI36
NG_009791.1:g.12238G= , LRG_69:g.12238G=

Transcript Alleles

HGVS Amino-acid Change
XR_938075.1:n.712C=
XR_938076.1:n.777C=
XR_938078.1:n.676C=
XR_938079.1:n.569C=
XR_938075.2:n.1296C=
XR_938078.2:n.1260C=