Canonical Allele Identifier: CA2246165946
Gene:

Linked Data

dbSNP Id: rs1981895832

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137705C>G , CM000679.2:g.8137705C>G GRCh38
NC_000017.10:g.8041023C>G , CM000679.1:g.8041023C>G GRCh37
NC_000017.9:g.7981748C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1144C>G
XR_934203.1:n.70-1772C>G
XR_934202.2:n.414-1144C>G