Canonical Allele Identifier: CA2129379097
Gene:

Linked Data

dbSNP Id: rs12588304

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384975T>G , CM000676.2:g.36384975T>G GRCh38
NC_000014.8:g.36854180T>G , CM000676.1:g.36854180T>G GRCh37
NC_000014.7:g.35923931T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12184T>G XP_011535730.1:n.319-12184T>G
XR_943756.1:n.358+23879T>G