Canonical Allele Identifier: CA2059285004
Gene:

Linked Data

dbSNP Id: rs1813700759

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501355G>A , CM000674.2:g.102501355G>A GRCh38
NC_000012.11:g.102895133G>A , CM000674.1:g.102895133G>A GRCh37
NC_000012.10:g.101419263G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17467G>A