Canonical Allele Identifier: CA953178829
Gene: TMEM132C HGNC NCBI

Linked Data

gnomAD v3: 12-128701923-A-G
gnomAD v4: 12-128701923-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128701923A>G , CM000674.2:g.128701923A>G GRCh38
NC_000012.11:g.129186468A>G , CM000674.1:g.129186468A>G GRCh37
NC_000012.10:g.127752421A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000435159.3:c.2122-3167A>G MANE Select ENSP00000410852.2:n.2122-3167A>G
ENST00000435159.2:c.2122-3167A>G ENSP00000410852.2:n.2122-3167A>G
NM_001136103.2:c.2122-3167A>G NP_001129575.2:n.2122-3167A>G
XM_011538998.1:c.2062-3167A>G XP_011537300.1:n.2062-3167A>G
XM_011538998.2:c.2062-3167A>G XP_011537300.1:n.2062-3167A>G
XR_001748922.1:n.2355-2729A>G
NM_001136103.3:c.2122-3167A>G MANE Select NP_001129575.2:n.2122-3167A>G
NM_001387058.1:c.2062-3167A>G NP_001373987.1:n.2062-3167A>G
Search 100 bp 5'
Search 100 bp 3'