Canonical Allele Identifier: CA15858305
Gene:

Linked Data

dbSNP Id: rs11636802

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.56483399A>G , CM000677.2:g.56483399A>G GRCh38
NC_000015.9:g.56775597A>G , CM000677.1:g.56775597A>G GRCh37
NC_000015.8:g.54562889A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932280.1:n.287T>C
XR_001751770.1:n.3440T>C