Canonical Allele Identifier: CA730295531
Gene:

Linked Data

dbSNP Id: rs1448852532

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036578T>G , CM000663.2:g.2036578T>G GRCh38
NC_000001.10:g.1968017T>G , CM000663.1:g.1968017T>G GRCh37
NC_000001.9:g.1957877T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.630A>C
XR_001737845.2:n.633A>C
XR_946823.3:n.633A>C