Canonical Allele Identifier: CA2246165905
Gene:

Linked Data

dbSNP Id: rs1981893862

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137581A>G , CM000679.2:g.8137581A>G GRCh38
NC_000017.10:g.8040899A>G , CM000679.1:g.8040899A>G GRCh37
NC_000017.9:g.7981624A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1268A>G
XR_934203.1:n.70-1896A>G
XR_934202.2:n.414-1268A>G