Canonical Allele Identifier: CA259369486
Gene:

Linked Data

dbSNP Id: rs1045906678

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384932G>T , CM000676.2:g.36384932G>T GRCh38
NC_000014.8:g.36854137G>T , CM000676.1:g.36854137G>T GRCh37
NC_000014.7:g.35923888G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12227G>T XP_011535730.1:n.319-12227G>T
XR_943756.1:n.358+23836G>T