Canonical Allele Identifier: CA239298346
Gene:

Linked Data

dbSNP Id: rs913848552

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004882G>A , CM000674.2:g.76004882G>A GRCh38
NC_000012.11:g.76398662G>A , CM000674.1:g.76398662G>A GRCh37
NC_000012.10:g.74684929G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945110.1:n.311+1307C>T
XR_001749218.2:n.403-1305C>T
XR_945110.3:n.402+1307C>T