Canonical Allele Identifier: CA685188111
Gene: TMEM132C HGNC NCBI

Linked Data

dbSNP Id: rs1193333245
gnomAD v3: 12-128701592-T-C
gnomAD v4: 12-128701592-T-C
MyVariant Identifiers: chr12:g.129186137T>C (hg19) chr12:g.128701592T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701592T>C , CM000674.2:g.128701592T>C GRCh38
NC_000012.11:g.129186137T>C , CM000674.1:g.129186137T>C GRCh37
NC_000012.10:g.127752090T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.2122-3498T>C MANE Select ENSP00000410852.2:n.2122-3498T>C
ENST00000435159.2:c.2122-3498T>C ENSP00000410852.2:n.2122-3498T>C
NM_001136103.2:c.2122-3498T>C NP_001129575.2:n.2122-3498T>C
XM_011538998.1:c.2062-3498T>C XP_011537300.1:n.2062-3498T>C
XM_011538998.2:c.2062-3498T>C XP_011537300.1:n.2062-3498T>C
XR_001748922.1:n.2355-3060T>C
NM_001136103.3:c.2122-3498T>C MANE Select NP_001129575.2:n.2122-3498T>C
NM_001387058.1:c.2062-3498T>C NP_001373987.1:n.2062-3498T>C
Search 100 bp 5'
Search 100 bp 3'