Canonical Allele Identifier: CA63947648

Gene: TMEM237

Linked Data

• dbSNP Id: rs998487230
• gnomAD v3: 2-201620724-G-T
• gnomAD v4: 2-201620724-G-T
• MyVariant Identifiers: chr2:g.202485447G>T (hg19) ; chr2:g.201620724G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201620724G>T , CM000664.2:g.201620724G>T	GRCh38
NC_000002.11:g.202485447G>T , CM000664.1:g.202485447G>T	GRCh37
NC_000002.10:g.202193692G>T	NCBI36
NG_032049.1:g.27806C>A
NG_051007.1:g.3459C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000621467.5:c.*3531C>A	ENSP00000480508.2:n.*3531C>A
ENST00000686475.1:n.4698C>A
ENST00000409883.7:c.*3531C>A MANE Select	ENSP00000386264.2:n.*3531C>A
ENST00000409444.6:c.*3531C>A	ENSP00000387203.2:n.*3531C>A
ENST00000409883.6:c.*3531C>A	ENSP00000386264.2:n.*3531C>A
ENST00000495329.1:n.3897C>A
NM_001044385.2:c.*3531C>A	NP_001037850.1:n.*3531C>A
NM_152388.3:c.*3531C>A	NP_689601.2:n.*3531C>A
NM_001044385.3:c.*3531C>A MANE Select	NP_001037850.1:n.*3531C>A
NM_152388.4:c.*3531C>A	NP_689601.2:n.*3531C>A