Canonical Allele Identifier: CA2129379086
Gene:

Linked Data

dbSNP Id: rs1566573713

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384950T>C , CM000676.2:g.36384950T>C GRCh38
NC_000014.8:g.36854155T>C , CM000676.1:g.36854155T>C GRCh37
NC_000014.7:g.35923906T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12209T>C XP_011535730.1:n.319-12209T>C
XR_943756.1:n.358+23854T>C