Canonical Allele Identifier: CA1224246965
Gene:

Linked Data

dbSNP Id: rs1691409858

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224886967C>G , CM000663.2:g.224886967C>G GRCh38
NC_000001.10:g.225074669C>G , CM000663.1:g.225074669C>G GRCh37
NC_000001.9:g.223141292C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949207.1:n.66-2186G>C
XR_949207.2:n.63-2186G>C