Canonical Allele Identifier: CA2056601

Gene: TMEM237

Linked Data

• dbSNP Id: rs745908076
• ExAC: 2:202504964 T / C
• gnomAD v2: 2-202504964-T-C
• gnomAD v3: 2-201640241-T-C
• gnomAD v4: 2-201640241-T-C
• MyVariant Identifiers: chr2:g.202504964T>C (hg19) ; chr2:g.201640241T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201640241T>C , CM000664.2:g.201640241T>C	GRCh38
NC_000002.11:g.202504964T>C , CM000664.1:g.202504964T>C	GRCh37
NC_000002.10:g.202213209T>C	NCBI36
NG_032049.1:g.8289A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.-356+652A>G	ENSP00000480508.2:n.-356+652A>G
ENST00000409883.7:c.79+20A>G MANE Select	ENSP00000386264.2:n.79+20A>G
ENST00000286196.9:c.-1+652A>G	ENSP00000286196.5:n.-1+652A>G
ENST00000409444.6:c.55+20A>G	ENSP00000387203.2:n.55+20A>G
ENST00000409883.6:c.79+20A>G	ENSP00000386264.2:n.79+20A>G
ENST00000432684.6:c.79+20A>G	ENSP00000413230.2:n.79+20A>G
ENST00000444047.6:c.79+20A>G	ENSP00000402681.2:n.79+20A>G
ENST00000463205.2:n.82+20A>G
ENST00000489550.5:n.92+652A>G
ENST00000621467.4:c.50+652A>G	ENSP00000480508.1:n.50+652A>G
NM_001044385.2:c.79+20A>G	NP_001037850.1:n.79+20A>G
NM_152388.3:c.55+20A>G	NP_689601.2:n.55+20A>G
NM_001044385.3:c.79+20A>G MANE Select	NP_001037850.1:n.79+20A>G
NM_152388.4:c.55+20A>G	NP_689601.2:n.55+20A>G