Canonical Allele Identifier: CA513685646
Gene:

Linked Data

MyVariant Identifiers: chr22:g.23915279A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573092A>C , CM000684.2:g.23573092A>C GRCh38
NC_000022.10:g.23915279A>C , CM000684.1:g.23915279A>C GRCh37
NC_000022.9:g.22245279A>C NCBI36
NG_009791.1:g.12217T>G , LRG_69:g.12217T>G

Transcript Alleles

HGVS Amino-acid Change
XR_938078.1:n.697A>C
XR_938078.2:n.1281A>C