Canonical Allele Identifier: CA513685569
Gene:

Linked Data

MyVariant Identifiers: chr22:g.23915253A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573066A>G , CM000684.2:g.23573066A>G GRCh38
NC_000022.10:g.23915253A>G , CM000684.1:g.23915253A>G GRCh37
NC_000022.9:g.22245253A>G NCBI36
NG_009791.1:g.12243T>C , LRG_69:g.12243T>C

Transcript Alleles

HGVS Amino-acid Change
XR_938075.1:n.707A>G
XR_938076.1:n.772A>G
XR_938078.1:n.671A>G
XR_938079.1:n.564A>G
XR_938075.2:n.1291A>G
XR_938078.2:n.1255A>G