Canonical Allele Identifier: CA605833772
Gene:

Linked Data

dbSNP Id: rs1166852957

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004957G>T , CM000674.2:g.76004957G>T GRCh38
NC_000012.11:g.76398737G>T , CM000674.1:g.76398737G>T GRCh37
NC_000012.10:g.74685004G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945110.1:n.311+1232C>A
XR_001749218.2:n.402+1232C>A
XR_945110.3:n.402+1232C>A