Canonical Allele Identifier: CA2071304277
Gene: TMEM132C HGNC NCBI

Linked Data

dbSNP Id: rs1876592153
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128610415T>A , CM000674.2:g.128610415T>A GRCh38
NC_000012.11:g.129094960T>A , CM000674.1:g.129094960T>A GRCh37
NC_000012.10:g.127660913T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.1122-5737T>A MANE Select ENSP00000410852.2:n.1122-5737T>A
ENST00000435159.2:c.1122-5737T>A ENSP00000410852.2:n.1122-5737T>A
NM_001136103.2:c.1122-5737T>A NP_001129575.2:n.1122-5737T>A
XM_011538998.1:c.1062-5737T>A XP_011537300.1:n.1062-5737T>A
XM_011538998.2:c.1062-5737T>A XP_011537300.1:n.1062-5737T>A
XR_001748922.1:n.1355-5737T>A
NM_001136103.3:c.1122-5737T>A MANE Select NP_001129575.2:n.1122-5737T>A
NM_001387058.1:c.1062-5737T>A NP_001373987.1:n.1062-5737T>A
Search 100 bp 5'
Search 100 bp 3'