Canonical Allele Identifier: CA513685582
Gene:

Linked Data

MyVariant Identifiers: chr22:g.23915257C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573070C>G , CM000684.2:g.23573070C>G GRCh38
NC_000022.10:g.23915257C>G , CM000684.1:g.23915257C>G GRCh37
NC_000022.9:g.22245257C>G NCBI36
NG_009791.1:g.12239G>C , LRG_69:g.12239G>C

Transcript Alleles

HGVS Amino-acid Change
XR_938075.1:n.711C>G
XR_938076.1:n.776C>G
XR_938078.1:n.675C>G
XR_938079.1:n.568C>G
XR_938075.2:n.1295C>G
XR_938078.2:n.1259C>G