Canonical Allele Identifier: CA538945396

Gene: TMEM237

Linked Data

• dbSNP Id: rs1459892137
• gnomAD v2: 2-202488218-T-C
• gnomAD v3: 2-201623495-T-C
• gnomAD v4: 2-201623495-T-C
• MyVariant Identifiers: chr2:g.202488218T>C (hg19) ; chr2:g.201623495T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623495T>C , CM000664.2:g.201623495T>C	GRCh38
NC_000002.11:g.202488218T>C , CM000664.1:g.202488218T>C	GRCh37
NC_000002.10:g.202196463T>C	NCBI36
NG_032049.1:g.25035A>G
NG_051007.1:g.688A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*760A>G	ENSP00000480508.2:n.*760A>G
ENST00000686475.1:n.1927A>G
ENST00000409883.7:c.*760A>G MANE Select	ENSP00000386264.2:n.*760A>G
ENST00000409444.6:c.*760A>G	ENSP00000387203.2:n.*760A>G
ENST00000409883.6:c.*760A>G	ENSP00000386264.2:n.*760A>G
ENST00000495329.1:n.1126A>G
NM_001044385.2:c.*760A>G	NP_001037850.1:n.*760A>G
NM_152388.3:c.*760A>G	NP_689601.2:n.*760A>G
NM_001044385.3:c.*760A>G MANE Select	NP_001037850.1:n.*760A>G
NM_152388.4:c.*760A>G	NP_689601.2:n.*760A>G