Canonical Allele Identifier: CA1149397033
Gene:

Linked Data

dbSNP Id: rs987645384

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036575C>G , CM000663.2:g.2036575C>G GRCh38
NC_000001.10:g.1968014C>G , CM000663.1:g.1968014C>G GRCh37
NC_000001.9:g.1957874C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946823.1:n.633G>C
XR_001737845.2:n.636G>C
XR_946823.3:n.636G>C