Canonical Allele Identifier: CA2071351270

Gene: TMEM132C

Linked Data

• dbSNP Id: rs2398418

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128702093T>G , CM000674.2:g.128702093T>G	GRCh38
NC_000012.11:g.129186638T>G , CM000674.1:g.129186638T>G	GRCh37
NC_000012.10:g.127752591T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435159.3:c.2122-2997T>G MANE Select	ENSP00000410852.2:n.2122-2997T>G
ENST00000435159.2:c.2122-2997T>G	ENSP00000410852.2:n.2122-2997T>G
NM_001136103.2:c.2122-2997T>G	NP_001129575.2:n.2122-2997T>G
XM_011538998.1:c.2062-2997T>G	XP_011537300.1:n.2062-2997T>G
XM_011538998.2:c.2062-2997T>G	XP_011537300.1:n.2062-2997T>G
XR_001748922.1:n.2355-2559T>G
NM_001136103.3:c.2122-2997T>G MANE Select	NP_001129575.2:n.2122-2997T>G
NM_001387058.1:c.2062-2997T>G	NP_001373987.1:n.2062-2997T>G