Canonical Allele Identifier: CA63949639

Gene: TMEM237

Linked Data

• dbSNP Id: rs540321745
• gnomAD v3: 2-201623484-G-A
• gnomAD v4: 2-201623484-G-A
• MyVariant Identifiers: chr2:g.202488207G>A (hg19) ; chr2:g.201623484G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623484G>A , CM000664.2:g.201623484G>A	GRCh38
NC_000002.11:g.202488207G>A , CM000664.1:g.202488207G>A	GRCh37
NC_000002.10:g.202196452G>A	NCBI36
NG_032049.1:g.25046C>T
NG_051007.1:g.699C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*771C>T	ENSP00000480508.2:n.*771C>T
ENST00000686475.1:n.1938C>T
ENST00000409883.7:c.*771C>T MANE Select	ENSP00000386264.2:n.*771C>T
ENST00000409444.6:c.*771C>T	ENSP00000387203.2:n.*771C>T
ENST00000409883.6:c.*771C>T	ENSP00000386264.2:n.*771C>T
ENST00000495329.1:n.1137C>T
NM_001044385.2:c.*771C>T	NP_001037850.1:n.*771C>T
NM_152388.3:c.*771C>T	NP_689601.2:n.*771C>T
NM_001044385.3:c.*771C>T MANE Select	NP_001037850.1:n.*771C>T
NM_152388.4:c.*771C>T	NP_689601.2:n.*771C>T