Canonical Allele Identifier: CA2059285059
Gene:

Linked Data

dbSNP Id: rs1881755654

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501474A>C , CM000674.2:g.102501474A>C GRCh38
NC_000012.11:g.102895252A>C , CM000674.1:g.102895252A>C GRCh37
NC_000012.10:g.101419382A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17586A>C