Canonical Allele Identifier: CA350304912

Gene: TMEM237

Linked Data

• gnomAD v4: 2-201626149-T-C
• MyVariant Identifiers: chr2:g.202490872T>C (hg19) ; chr2:g.201626149T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201626149T>C , CM000664.2:g.201626149T>C	GRCh38
NC_000002.11:g.202490872T>C , CM000664.1:g.202490872T>C	GRCh37
NC_000002.10:g.202199117T>C	NCBI36
NG_032049.1:g.22381A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471318.6:n.834-2A>G
ENST00000621467.5:c.912-2A>G	ENSP00000480508.2:n.912-2A>G
ENST00000686475.1:n.978-2A>G
ENST00000409883.7:c.1038-2A>G MANE Select	ENSP00000386264.2:n.1038-2A>G
ENST00000286196.9:c.*602-2A>G	ENSP00000286196.5:n.*602-2A>G
ENST00000409444.6:c.1014-2A>G	ENSP00000387203.2:n.1014-2A>G
ENST00000409883.6:c.1038-2A>G	ENSP00000386264.2:n.1038-2A>G
ENST00000471318.5:n.266-2A>G
ENST00000495329.1:n.175A>G
ENST00000621467.4:c.1014-2A>G	ENSP00000480508.1:n.1014-2A>G
NM_001044385.2:c.1038-2A>G	NP_001037850.1:n.1038-2A>G
NM_152388.3:c.1014-2A>G	NP_689601.2:n.1014-2A>G
NM_001044385.3:c.1038-2A>G MANE Select	NP_001037850.1:n.1038-2A>G
NM_152388.4:c.1014-2A>G	NP_689601.2:n.1014-2A>G