Canonical Allele Identifier: CA2662656994

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201623434-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623434G>C , CM000664.2:g.201623434G>C	GRCh38
NC_000002.11:g.202488157G>C , CM000664.1:g.202488157G>C	GRCh37
NC_000002.10:g.202196402G>C	NCBI36
NG_032049.1:g.25096C>G
NG_051007.1:g.749C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*821C>G	ENSP00000480508.2:n.*821C>G
ENST00000686475.1:n.1988C>G
ENST00000409883.7:c.*821C>G MANE Select	ENSP00000386264.2:n.*821C>G
ENST00000409444.6:c.*821C>G	ENSP00000387203.2:n.*821C>G
ENST00000409883.6:c.*821C>G	ENSP00000386264.2:n.*821C>G
ENST00000495329.1:n.1187C>G
NM_001044385.2:c.*821C>G	NP_001037850.1:n.*821C>G
NM_152388.3:c.*821C>G	NP_689601.2:n.*821C>G
NM_001044385.3:c.*821C>G MANE Select	NP_001037850.1:n.*821C>G
NM_152388.4:c.*821C>G	NP_689601.2:n.*821C>G