Canonical Allele Identifier: CA685188379

Gene: TMEM132C

Linked Data

• dbSNP Id: rs1326128716
• gnomAD v3: 12-128702092-G-T
• gnomAD v4: 12-128702092-G-T
• MyVariant Identifiers: chr12:g.129186637G>T (hg19) ; chr12:g.128702092G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128702092G>T , CM000674.2:g.128702092G>T	GRCh38
NC_000012.11:g.129186637G>T , CM000674.1:g.129186637G>T	GRCh37
NC_000012.10:g.127752590G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-2998G>T MANE Select	ENSP00000410852.2:n.2122-2998G>T
ENST00000435159.2:c.2122-2998G>T	ENSP00000410852.2:n.2122-2998G>T
NM_001136103.2:c.2122-2998G>T	NP_001129575.2:n.2122-2998G>T
XM_011538998.1:c.2062-2998G>T	XP_011537300.1:n.2062-2998G>T
XM_011538998.2:c.2062-2998G>T	XP_011537300.1:n.2062-2998G>T
XR_001748922.1:n.2355-2560G>T
NM_001136103.3:c.2122-2998G>T MANE Select	NP_001129575.2:n.2122-2998G>T
NM_001387058.1:c.2062-2998G>T	NP_001373987.1:n.2062-2998G>T