Canonical Allele Identifier: CA2129379130

Gene:

Linked Data

• dbSNP Id: rs1882064479

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36385059G>T , CM000676.2:g.36385059G>T	GRCh38
NC_000014.8:g.36854264G>T , CM000676.1:g.36854264G>T	GRCh37
NC_000014.7:g.35924015G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011537428.1:c.319-12100G>T	XP_011535730.1:n.319-12100G>T
XR_943756.1:n.358+23963G>T