Canonical Allele Identifier: CA513685581
Gene:

Linked Data

MyVariant Identifiers: chr22:g.23915256A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573069A>G , CM000684.2:g.23573069A>G GRCh38
NC_000022.10:g.23915256A>G , CM000684.1:g.23915256A>G GRCh37
NC_000022.9:g.22245256A>G NCBI36
NG_009791.1:g.12240T>C , LRG_69:g.12240T>C

Transcript Alleles

HGVS Amino-acid Change
XR_938075.1:n.710A>G
XR_938076.1:n.775A>G
XR_938078.1:n.674A>G
XR_938079.1:n.567A>G
XR_938075.2:n.1294A>G
XR_938078.2:n.1258A>G