Canonical Allele Identifier: CA2071351053

Gene: TMEM132C

Linked Data

• dbSNP Id: rs1954804487

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128701655A>C , CM000674.2:g.128701655A>C	GRCh38
NC_000012.11:g.129186200A>C , CM000674.1:g.129186200A>C	GRCh37
NC_000012.10:g.127752153A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000435159.3:c.2122-3435A>C MANE Select	ENSP00000410852.2:n.2122-3435A>C
ENST00000435159.2:c.2122-3435A>C	ENSP00000410852.2:n.2122-3435A>C
NM_001136103.2:c.2122-3435A>C	NP_001129575.2:n.2122-3435A>C
XM_011538998.1:c.2062-3435A>C	XP_011537300.1:n.2062-3435A>C
XM_011538998.2:c.2062-3435A>C	XP_011537300.1:n.2062-3435A>C
XR_001748922.1:n.2355-2997A>C
NM_001136103.3:c.2122-3435A>C MANE Select	NP_001129575.2:n.2122-3435A>C
NM_001387058.1:c.2062-3435A>C	NP_001373987.1:n.2062-3435A>C