Canonical Allele Identifier: CA2129379071
Gene:

Linked Data

dbSNP Id: rs1566573691

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36384924A>T , CM000676.2:g.36384924A>T GRCh38
NC_000014.8:g.36854129A>T , CM000676.1:g.36854129A>T GRCh37
NC_000014.7:g.35923880A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537428.1:c.319-12235A>T XP_011535730.1:n.319-12235A>T
XR_943756.1:n.358+23828A>T