Canonical Allele Identifier: CA10612415
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 333535
ClinVar RCV Id: RCV000329126
dbSNP Id: rs886055437

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201621242T>C , CM000664.2:g.201621242T>C GRCh38
NC_000002.11:g.202485965T>C , CM000664.1:g.202485965T>C GRCh37
NC_000002.10:g.202194210T>C NCBI36
NG_032049.1:g.27288A>G
NG_051007.1:g.2941A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000409883.7:c.*3013A>G MANE Select ENSP00000386264.2:p.=
ENST00000409444.6:c.*3013A>G ENSP00000387203.2:p.=
ENST00000409883.6:c.*3013A>G ENSP00000386264.2:p.=
ENST00000495329.1:n.3379A>G
NM_001044385.2:c.*3013A>G NP_001037850.1:p.=
NM_152388.3:c.*3013A>G NP_689601.2:p.=
NM_001044385.3:c.*3013A>G MANE Select NP_001037850.1:p.=
NM_152388.4:c.*3013A>G NP_689601.2:p.=