Canonical Allele Identifier: CA2059285093
Gene:

Linked Data

dbSNP Id: rs372826494

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501537T>G , CM000674.2:g.102501537T>G GRCh38
NC_000012.11:g.102895315T>G , CM000674.1:g.102895315T>G GRCh37
NC_000012.10:g.101419445T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17649T>G