Canonical Allele Identifier: CA513685642
Gene:

Linked Data

dbSNP Id: rs1602286224
MyVariant Identifiers: chr22:g.23915277A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573090A>G , CM000684.2:g.23573090A>G GRCh38
NC_000022.10:g.23915277A>G , CM000684.1:g.23915277A>G GRCh37
NC_000022.9:g.22245277A>G NCBI36
NG_009791.1:g.12219T>C , LRG_69:g.12219T>C

Transcript Alleles

HGVS Amino-acid Change
XR_938078.1:n.695A>G
XR_938078.2:n.1279A>G