Canonical Allele Identifier: CA608136486
Gene: TMEM132C HGNC NCBI

Linked Data

dbSNP Id: rs1184039938
gnomAD v2: 12-129186629-G-C
gnomAD v3: 12-128702084-G-C
gnomAD v4: 12-128702084-G-C
MyVariant Identifiers: chr12:g.129186629G>C (hg19) chr12:g.128702084G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128702084G>C , CM000674.2:g.128702084G>C GRCh38
NC_000012.11:g.129186629G>C , CM000674.1:g.129186629G>C GRCh37
NC_000012.10:g.127752582G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.2122-3006G>C MANE Select ENSP00000410852.2:n.2122-3006G>C
ENST00000435159.2:c.2122-3006G>C ENSP00000410852.2:n.2122-3006G>C
NM_001136103.2:c.2122-3006G>C NP_001129575.2:n.2122-3006G>C
XM_011538998.1:c.2062-3006G>C XP_011537300.1:n.2062-3006G>C
XM_011538998.2:c.2062-3006G>C XP_011537300.1:n.2062-3006G>C
XR_001748922.1:n.2355-2568G>C
NM_001136103.3:c.2122-3006G>C MANE Select NP_001129575.2:n.2122-3006G>C
NM_001387058.1:c.2062-3006G>C NP_001373987.1:n.2062-3006G>C
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