Canonical Allele Identifier: CA1041261751

Gene: TMEM237

Linked Data

• dbSNP Id: rs1957704033
• gnomAD v3: 2-201621176-A-G
• gnomAD v4: 2-201621176-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201621176A>G , CM000664.2:g.201621176A>G	GRCh38
NC_000002.11:g.202485899A>G , CM000664.1:g.202485899A>G	GRCh37
NC_000002.10:g.202194144A>G	NCBI36
NG_032049.1:g.27354T>C
NG_051007.1:g.3007T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000621467.5:c.*3079T>C	ENSP00000480508.2:n.*3079T>C
ENST00000686475.1:n.4246T>C
ENST00000409883.7:c.*3079T>C MANE Select	ENSP00000386264.2:n.*3079T>C
ENST00000409444.6:c.*3079T>C	ENSP00000387203.2:n.*3079T>C
ENST00000409883.6:c.*3079T>C	ENSP00000386264.2:n.*3079T>C
ENST00000495329.1:n.3445T>C
NM_001044385.2:c.*3079T>C	NP_001037850.1:n.*3079T>C
NM_152388.3:c.*3079T>C	NP_689601.2:n.*3079T>C
NM_001044385.3:c.*3079T>C MANE Select	NP_001037850.1:n.*3079T>C
NM_152388.4:c.*3079T>C	NP_689601.2:n.*3079T>C