Canonical Allele Identifier: CA2056605

Gene: TMEM237

Linked Data

• dbSNP Id: rs763520106
• ExAC: 2:202504992 A / G
• gnomAD v2: 2-202504992-A-G
• gnomAD v4: 2-201640269-A-G
• MyVariant Identifiers: chr2:g.202504992A>G (hg19) ; chr2:g.201640269A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201640269A>G , CM000664.2:g.201640269A>G	GRCh38
NC_000002.11:g.202504992A>G , CM000664.1:g.202504992A>G	GRCh37
NC_000002.10:g.202213237A>G	NCBI36
NG_032049.1:g.8261T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000621467.5:c.-356+624T>C	ENSP00000480508.2:n.-356+624T>C
ENST00000409883.7:c.75-4T>C MANE Select	ENSP00000386264.2:n.75-4T>C
ENST00000286196.9:c.-1+624T>C	ENSP00000286196.5:n.-1+624T>C
ENST00000409444.6:c.51-4T>C	ENSP00000387203.2:n.51-4T>C
ENST00000409883.6:c.75-4T>C	ENSP00000386264.2:n.75-4T>C
ENST00000432684.6:c.75-4T>C	ENSP00000413230.2:n.75-4T>C
ENST00000444047.6:c.75-4T>C	ENSP00000402681.2:n.75-4T>C
ENST00000463205.2:n.78-4T>C
ENST00000489550.5:n.92+624T>C
ENST00000621467.4:c.50+624T>C	ENSP00000480508.1:n.50+624T>C
NM_001044385.2:c.75-4T>C	NP_001037850.1:n.75-4T>C
NM_152388.3:c.51-4T>C	NP_689601.2:n.51-4T>C
NM_001044385.3:c.75-4T>C MANE Select	NP_001037850.1:n.75-4T>C
NM_152388.4:c.51-4T>C	NP_689601.2:n.51-4T>C