Canonical Allele Identifier: CA245938369
Gene: TMEM132C HGNC NCBI

Linked Data

dbSNP Id: rs1056859743
gnomAD v2: 12-129095175-C-T
gnomAD v3: 12-128610630-C-T
gnomAD v4: 12-128610630-C-T
MyVariant Identifiers: chr12:g.129095175C>T (hg19) chr12:g.128610630C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128610630C>T , CM000674.2:g.128610630C>T GRCh38
NC_000012.11:g.129095175C>T , CM000674.1:g.129095175C>T GRCh37
NC_000012.10:g.127661128C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.1122-5522C>T MANE Select ENSP00000410852.2:n.1122-5522C>T
ENST00000435159.2:c.1122-5522C>T ENSP00000410852.2:n.1122-5522C>T
NM_001136103.2:c.1122-5522C>T NP_001129575.2:n.1122-5522C>T
XM_011538998.1:c.1062-5522C>T XP_011537300.1:n.1062-5522C>T
XM_011538998.2:c.1062-5522C>T XP_011537300.1:n.1062-5522C>T
XR_001748922.1:n.1355-5522C>T
NM_001136103.3:c.1122-5522C>T MANE Select NP_001129575.2:n.1122-5522C>T
NM_001387058.1:c.1062-5522C>T NP_001373987.1:n.1062-5522C>T
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