Canonical Allele Identifier: CA730295533
Gene:

Linked Data

dbSNP Id: rs1185484941

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036580C>T , CM000663.2:g.2036580C>T GRCh38
NC_000001.10:g.1968019C>T , CM000663.1:g.1968019C>T GRCh37
NC_000001.9:g.1957879C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.628G>A
XR_001737845.2:n.631G>A
XR_946823.3:n.631G>A