Canonical Allele Identifier: CA1223909945
Gene:

Linked Data

dbSNP Id: rs1571984672

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068688A>G , CM000663.2:g.224068688A>G GRCh38
NC_000001.10:g.224256390A>G , CM000663.1:g.224256390A>G GRCh37
NC_000001.9:g.222323013A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+1034A>G
XR_001737824.1:n.242+1034A>G