Canonical Allele Identifier: CA350304447

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201626076-C-A
• MyVariant Identifiers: chr2:g.202490799C>A (hg19) ; chr2:g.201626076C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626076C>A , CM000664.2:g.201626076C>A	GRCh38
NC_000002.11:g.202490799C>A , CM000664.1:g.202490799C>A	GRCh37
NC_000002.10:g.202199044C>A	NCBI36
NG_032049.1:g.22454G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.905G>T
ENST00000621467.5:c.983G>T	ENSP00000480508.2:p.Gly328Val
ENST00000686475.1:n.1049G>T
ENST00000409883.7:c.1109G>T MANE Select	ENSP00000386264.2:p.Gly370Val
ENST00000286196.9:c.*673G>T	ENSP00000286196.5:n.*673G>T
ENST00000409444.6:c.1085G>T	ENSP00000387203.2:p.Gly362Val
ENST00000409883.6:c.1109G>T	ENSP00000386264.2:p.Gly370Val
ENST00000471318.5:n.337G>T
ENST00000495329.1:n.248G>T
ENST00000621467.4:c.1085G>T	ENSP00000480508.1:p.Gly362Val
NM_001044385.2:c.1109G>T	NP_001037850.1:p.Gly370Val
NM_152388.3:c.1085G>T	NP_689601.2:p.Gly362Val
NM_001044385.3:c.1109G>T MANE Select	NP_001037850.1:p.Gly370Val
NM_152388.4:c.1085G>T	NP_689601.2:p.Gly362Val