Canonical Allele Identifier: CA16525122
Gene:

Linked Data

dbSNP Id: rs8062487

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.60439872T>C , CM000678.2:g.60439872T>C GRCh38
NC_000016.9:g.60473776T>C , CM000678.1:g.60473776T>C GRCh37
NC_000016.8:g.59031277T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_243457.2:n.376-32864T>C
XR_933651.1:n.539-32864T>C
XR_933652.1:n.602-32864T>C
XR_933653.1:n.313-32864T>C
XR_001752229.1:n.539-32864T>C
XR_001752230.1:n.516-32864T>C
XR_001752231.1:n.313-32864T>C
XR_002957906.1:n.804-32864T>C