Canonical Allele Identifier: CA613506525
Gene:

Linked Data

dbSNP Id: rs1231162390

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384909G>C , CM000676.2:g.36384909G>C GRCh38
NC_000014.8:g.36854114G>C , CM000676.1:g.36854114G>C GRCh37
NC_000014.7:g.35923865G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12250G>C XP_011535730.1:n.319-12250G>C
XR_943756.1:n.358+23813G>C