Canonical Allele Identifier: CA538946326

Gene: TMEM237

Linked Data

• dbSNP Id: rs1363677196
• gnomAD v2: 2-202490732-T-A
• gnomAD v4: 2-201626009-T-A
• MyVariant Identifiers: chr2:g.202490732T>A (hg19) ; chr2:g.201626009T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626009T>A , CM000664.2:g.201626009T>A	GRCh38
NC_000002.11:g.202490732T>A , CM000664.1:g.202490732T>A	GRCh37
NC_000002.10:g.202198977T>A	NCBI36
NG_032049.1:g.22521A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+17A>T
ENST00000621467.5:c.1033+17A>T	ENSP00000480508.2:n.1033+17A>T
ENST00000686475.1:n.1099+17A>T
ENST00000409883.7:c.1159+17A>T MANE Select	ENSP00000386264.2:n.1159+17A>T
ENST00000286196.9:c.*723+17A>T	ENSP00000286196.5:n.*723+17A>T
ENST00000409444.6:c.1135+17A>T	ENSP00000387203.2:n.1135+17A>T
ENST00000409883.6:c.1159+17A>T	ENSP00000386264.2:n.1159+17A>T
ENST00000471318.5:n.387+17A>T
ENST00000495329.1:n.298+17A>T
ENST00000621467.4:c.1135+17A>T	ENSP00000480508.1:n.1135+17A>T
NM_001044385.2:c.1159+17A>T	NP_001037850.1:n.1159+17A>T
NM_152388.3:c.1135+17A>T	NP_689601.2:n.1135+17A>T
NM_001044385.3:c.1159+17A>T MANE Select	NP_001037850.1:n.1159+17A>T
NM_152388.4:c.1135+17A>T	NP_689601.2:n.1135+17A>T