Canonical Allele Identifier: CA1041263178

Gene: TMEM237

Linked Data

• dbSNP Id: rs755985117
• gnomAD v3: 2-201625999-T-C
• gnomAD v4: 2-201625999-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201625999T>C , CM000664.2:g.201625999T>C	GRCh38
NC_000002.11:g.202490722T>C , CM000664.1:g.202490722T>C	GRCh37
NC_000002.10:g.202198967T>C	NCBI36
NG_032049.1:g.22531A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.955+27A>G
ENST00000621467.5:c.1033+27A>G	ENSP00000480508.2:n.1033+27A>G
ENST00000686475.1:n.1099+27A>G
ENST00000409883.7:c.1159+27A>G MANE Select	ENSP00000386264.2:n.1159+27A>G
ENST00000286196.9:c.*723+27A>G	ENSP00000286196.5:n.*723+27A>G
ENST00000409444.6:c.1135+27A>G	ENSP00000387203.2:n.1135+27A>G
ENST00000409883.6:c.1159+27A>G	ENSP00000386264.2:n.1159+27A>G
ENST00000471318.5:n.387+27A>G
ENST00000495329.1:n.298+27A>G
ENST00000621467.4:c.1135+27A>G	ENSP00000480508.1:n.1135+27A>G
NM_001044385.2:c.1159+27A>G	NP_001037850.1:n.1159+27A>G
NM_152388.3:c.1135+27A>G	NP_689601.2:n.1135+27A>G
NM_001044385.3:c.1159+27A>G MANE Select	NP_001037850.1:n.1159+27A>G
NM_152388.4:c.1135+27A>G	NP_689601.2:n.1135+27A>G