Canonical Allele Identifier: CA2726851573
Gene:

Linked Data

dbSNP Id: rs2121328929

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293163C>A , CM000674.2:g.93293163C>A GRCh38
NC_000012.11:g.93686939C>A , CM000674.1:g.93686939C>A GRCh37
NC_000012.10:g.92211070C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34864G>T