Canonical Allele Identifier: CA2056707
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 257311
dbSNP Id: rs113186360

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201643412C>T , CM000664.2:g.201643412C>T GRCh38
NC_000002.11:g.202508135C>T , CM000664.1:g.202508135C>T GRCh37
NC_000002.10:g.202216380C>T NCBI36
NG_012654.1:g.60283G>A
NG_032049.1:g.5118G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000409883.7:c.-12G>A MANE Select ENSP00000386264.2:n.-12G>A
ENST00000286196.9:c.-86G>A ENSP00000286196.5:n.-86G>A
ENST00000409883.6:c.-12G>A ENSP00000386264.2:n.-12G>A
ENST00000432684.6:c.-12G>A ENSP00000413230.2:n.-12G>A
ENST00000489550.5:n.7G>A
NM_001044385.2:c.-12G>A NP_001037850.1:n.-12G>A
NM_001044385.3:c.-12G>A MANE Select NP_001037850.1:n.-12G>A