Canonical Allele Identifier: CA2059284965
Gene:

Linked Data

dbSNP Id: rs1881752132

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501298G>A , CM000674.2:g.102501298G>A GRCh38
NC_000012.11:g.102895076G>A , CM000674.1:g.102895076G>A GRCh37
NC_000012.10:g.101419206G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17410G>A