Canonical Allele Identifier: CA2059284981
Gene:

Linked Data

dbSNP Id: rs1592850255

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501322C>A , CM000674.2:g.102501322C>A GRCh38
NC_000012.11:g.102895100C>A , CM000674.1:g.102895100C>A GRCh37
NC_000012.10:g.101419230C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749289.1:n.1952+17434C>A