Canonical Allele Identifier: CA245938348
Gene: TMEM132C HGNC NCBI

Linked Data

dbSNP Id: rs760802918
gnomAD v2: 12-129094915-C-T
gnomAD v3: 12-128610370-C-T
gnomAD v4: 12-128610370-C-T
MyVariant Identifiers: chr12:g.129094915C>T (hg19) chr12:g.128610370C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128610370C>T , CM000674.2:g.128610370C>T GRCh38
NC_000012.11:g.129094915C>T , CM000674.1:g.129094915C>T GRCh37
NC_000012.10:g.127660868C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435159.3:c.1122-5782C>T MANE Select ENSP00000410852.2:n.1122-5782C>T
ENST00000435159.2:c.1122-5782C>T ENSP00000410852.2:n.1122-5782C>T
NM_001136103.2:c.1122-5782C>T NP_001129575.2:n.1122-5782C>T
XM_011538998.1:c.1062-5782C>T XP_011537300.1:n.1062-5782C>T
XM_011538998.2:c.1062-5782C>T XP_011537300.1:n.1062-5782C>T
XR_001748922.1:n.1355-5782C>T
NM_001136103.3:c.1122-5782C>T MANE Select NP_001129575.2:n.1122-5782C>T
NM_001387058.1:c.1062-5782C>T NP_001373987.1:n.1062-5782C>T
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