Canonical Allele Identifier: CA513685607
Gene:

Linked Data

MyVariant Identifiers: chr22:g.23915265A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573078A>G , CM000684.2:g.23573078A>G GRCh38
NC_000022.10:g.23915265A>G , CM000684.1:g.23915265A>G GRCh37
NC_000022.9:g.22245265A>G NCBI36
NG_009791.1:g.12231T>C , LRG_69:g.12231T>C

Transcript Alleles

HGVS Amino-acid Change
XR_938078.1:n.683A>G
XR_938078.2:n.1267A>G