Canonical Allele Identifier: CA322555672
Gene:

Linked Data

dbSNP Id: rs550350212

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573086C>G , CM000684.2:g.23573086C>G GRCh38
NC_000022.10:g.23915273C>G , CM000684.1:g.23915273C>G GRCh37
NC_000022.9:g.22245273C>G NCBI36
NG_009791.1:g.12223G>C , LRG_69:g.12223G>C

Transcript Alleles

HGVS Amino-acid Change
XR_938078.1:n.691C>G
XR_938078.2:n.1275C>G