Canonical Allele Identifier: CA513685619
Gene:

Linked Data

MyVariant Identifiers: chr22:g.23915269A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573082A>G , CM000684.2:g.23573082A>G GRCh38
NC_000022.10:g.23915269A>G , CM000684.1:g.23915269A>G GRCh37
NC_000022.9:g.22245269A>G NCBI36
NG_009791.1:g.12227T>C , LRG_69:g.12227T>C

Transcript Alleles

HGVS Amino-acid Change
XR_938078.1:n.687A>G
XR_938078.2:n.1271A>G