Canonical Allele Identifier: CA1427630020
Gene:

Linked Data

dbSNP Id: rs1715479930

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187931699C>A , CM000665.2:g.187931699C>A GRCh38
NC_000003.11:g.187649487C>A , CM000665.1:g.187649487C>A GRCh37
NC_000003.10:g.189132181C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924814.1:n.1215G>T