Canonical Allele Identifier: CA2071351258
Gene: TMEM132C HGNC NCBI

Linked Data

dbSNP Id: rs1954808079
gnomAD v3: 12-128702078-T-C
gnomAD v4: 12-128702078-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128702078T>C , CM000674.2:g.128702078T>C GRCh38
NC_000012.11:g.129186623T>C , CM000674.1:g.129186623T>C GRCh37
NC_000012.10:g.127752576T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.2122-3012T>C MANE Select ENSP00000410852.2:n.2122-3012T>C
ENST00000435159.2:c.2122-3012T>C ENSP00000410852.2:n.2122-3012T>C
NM_001136103.2:c.2122-3012T>C NP_001129575.2:n.2122-3012T>C
XM_011538998.1:c.2062-3012T>C XP_011537300.1:n.2062-3012T>C
XM_011538998.2:c.2062-3012T>C XP_011537300.1:n.2062-3012T>C
XR_001748922.1:n.2355-2574T>C
NM_001136103.3:c.2122-3012T>C MANE Select NP_001129575.2:n.2122-3012T>C
NM_001387058.1:c.2062-3012T>C NP_001373987.1:n.2062-3012T>C
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