Canonical Allele Identifier: CA117764808
Gene:

Linked Data

dbSNP Id: rs1046417127

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.41107390G>A , CM000667.2:g.41107390G>A GRCh38
NC_000005.9:g.41107492G>A , CM000667.1:g.41107492G>A GRCh37
NC_000005.8:g.41143249G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925944.1:n.618-5238G>A
XR_925945.1:n.125-5238G>A
XR_925946.1:n.576-5238G>A
XR_925948.1:n.618-5238G>A
XR_001742650.1:n.618-5238G>A
XR_001742651.1:n.131-5238G>A