Canonical Allele Identifier: CA2726623576
Gene:

Linked Data

dbSNP Id: rs2136914293

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004861G>A , CM000674.2:g.76004861G>A GRCh38
NC_000012.11:g.76398641G>A , CM000674.1:g.76398641G>A GRCh37
NC_000012.10:g.74684908G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945110.1:n.311+1328C>T
XR_001749218.2:n.403-1284C>T
XR_945110.3:n.402+1328C>T