Canonical Allele Identifier: CA2059284971
Gene:

Linked Data

dbSNP Id: rs1592850253

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501308A>C , CM000674.2:g.102501308A>C GRCh38
NC_000012.11:g.102895086A>C , CM000674.1:g.102895086A>C GRCh37
NC_000012.10:g.101419216A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749289.1:n.1952+17420A>C