Canonical Allele Identifier: CA513685563
Gene:

Linked Data

MyVariant Identifiers: chr22:g.23915251T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573064T>G , CM000684.2:g.23573064T>G GRCh38
NC_000022.10:g.23915251T>G , CM000684.1:g.23915251T>G GRCh37
NC_000022.9:g.22245251T>G NCBI36
NG_009791.1:g.12245A>C , LRG_69:g.12245A>C

Transcript Alleles

HGVS Amino-acid Change
XR_938075.1:n.705T>G
XR_938076.1:n.770T>G
XR_938078.1:n.669T>G
XR_938079.1:n.562T>G
XR_938075.2:n.1289T>G
XR_938078.2:n.1253T>G