Canonical Allele Identifier: CA2378344908
Gene:

Linked Data

dbSNP Id: rs1601108901

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.15440814C>A , CM000683.2:g.15440814C>A GRCh38
NC_000021.8:g.16813133C>A , CM000683.1:g.16813133C>A GRCh37
NC_000021.7:g.15735004C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937593.1:n.552+412G>T
XR_001754965.2:n.468+3210G>T
XR_001754970.2:n.468+3210G>T
XR_001754971.2:n.468+3210G>T