Canonical Allele Identifier: CA2566698464
Gene: TMEM132D HGNC NCBI

Linked Data

dbSNP Id: rs1349212240
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.129162055G>T , CM000674.2:g.129162055G>T GRCh38
NC_000012.11:g.129646600G>T , CM000674.1:g.129646600G>T GRCh37
NC_000012.10:g.128212553G>T NCBI36
NG_052808.1:g.746613C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000422113.7:c.1443+47465C>A MANE Select ENSP00000408581.2:n.1443+47465C>A
ENST00000422113.6:c.1443+47465C>A ENSP00000408581.2:n.1443+47465C>A
ENST00000619366.1:c.1383+47465C>A ENSP00000478824.1:n.1383+47465C>A
NM_133448.2:c.1443+47465C>A NP_597705.2:n.1443+47465C>A
XM_011537894.1:c.1296+47465C>A XP_011536196.1:n.1296+47465C>A
NM_133448.3:c.1443+47465C>A MANE Select NP_597705.2:n.1443+47465C>A
Search 100 bp 5'
Search 100 bp 3'