Canonical Allele Identifier: CA2056297
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 257315
dbSNP Id: rs77570029

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201626051A>G , CM000664.2:g.201626051A>G GRCh38
NC_000002.11:g.202490774A>G , CM000664.1:g.202490774A>G GRCh37
NC_000002.10:g.202199019A>G NCBI36
NG_032049.1:g.22479T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000471318.6:n.930T>C
ENST00000621467.5:c.1008T>C ENSP00000480508.2:p.Tyr336=
ENST00000686475.1:n.1074T>C
ENST00000409883.7:c.1134T>C MANE Select ENSP00000386264.2:p.Tyr378=
ENST00000286196.9:c.*698T>C ENSP00000286196.5:n.*698T>C
ENST00000409444.6:c.1110T>C ENSP00000387203.2:p.Tyr370=
ENST00000409883.6:c.1134T>C ENSP00000386264.2:p.Tyr378=
ENST00000471318.5:n.362T>C
ENST00000495329.1:n.273T>C
ENST00000621467.4:c.1110T>C ENSP00000480508.1:p.Tyr370=
NM_001044385.2:c.1134T>C NP_001037850.1:p.Tyr378=
NM_152388.3:c.1110T>C NP_689601.2:p.Tyr370=
NM_001044385.3:c.1134T>C MANE Select NP_001037850.1:p.Tyr378=
NM_152388.4:c.1110T>C NP_689601.2:p.Tyr370=