Canonical Allele Identifier: CA2246165921
Gene:

Linked Data

dbSNP Id: rs1981894582

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137629A>G , CM000679.2:g.8137629A>G GRCh38
NC_000017.10:g.8040947A>G , CM000679.1:g.8040947A>G GRCh37
NC_000017.9:g.7981672A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_934202.1:n.183-1220A>G
XR_934203.1:n.70-1848A>G
XR_934202.2:n.414-1220A>G