Canonical Allele Identifier: CA2725394169
Gene:

Linked Data

dbSNP Id: rs2120863497

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5284240A>G , CM000674.2:g.5284240A>G GRCh38
NC_000012.11:g.5393406A>G , CM000674.1:g.5393406A>G GRCh37
NC_000012.10:g.5263667A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931576.1:n.611+7351A>G
XR_931577.1:n.611+7351A>G
XR_001748970.1:n.594+7351A>G