Canonical Allele Identifier: CA727900675
Gene:

Linked Data

dbSNP Id: rs1437784249

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237056G>A , CM000679.2:g.30237056G>A GRCh38
NC_000017.10:g.28564074G>A , CM000679.1:g.28564074G>A GRCh37
NC_000017.9:g.25588200G>A NCBI36
NG_011747.2:g.3881C>T

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.151G>A
XR_001752824.1:n.266G>A