Canonical Allele Identifier: CA2733190070
Gene:

Linked Data

dbSNP Id: rs2151857619

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137318G>A , CM000679.2:g.8137318G>A GRCh38
NC_000017.10:g.8040636G>A , CM000679.1:g.8040636G>A GRCh37
NC_000017.9:g.7981361G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1531G>A
XR_934203.1:n.70-2159G>A
XR_934202.2:n.414-1531G>A