Canonical Allele Identifier: CA2397855719
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573080G= , CM000684.2:g.23573080G= GRCh38
NC_000022.10:g.23915267G= , CM000684.1:g.23915267G= GRCh37
NC_000022.9:g.22245267G= NCBI36
NG_009791.1:g.12229C= , LRG_69:g.12229C=

Transcript Alleles

HGVS Amino-acid Change
XR_938078.1:n.685G=
XR_938078.2:n.1269G=