Canonical Allele Identifier: CA1041262336
Gene: TMEM237 HGNC NCBI

Linked Data

dbSNP Id: rs1957728835
gnomAD v3: 2-201623456-T-G
gnomAD v4: 2-201623456-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201623456T>G , CM000664.2:g.201623456T>G GRCh38
NC_000002.11:g.202488179T>G , CM000664.1:g.202488179T>G GRCh37
NC_000002.10:g.202196424T>G NCBI36
NG_032049.1:g.25074A>C
NG_051007.1:g.727A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000621467.5:c.*799A>C ENSP00000480508.2:n.*799A>C
ENST00000686475.1:n.1966A>C
ENST00000409883.7:c.*799A>C MANE Select ENSP00000386264.2:n.*799A>C
ENST00000409444.6:c.*799A>C ENSP00000387203.2:n.*799A>C
ENST00000409883.6:c.*799A>C ENSP00000386264.2:n.*799A>C
ENST00000495329.1:n.1165A>C
NM_001044385.2:c.*799A>C NP_001037850.1:n.*799A>C
NM_152388.3:c.*799A>C NP_689601.2:n.*799A>C
NM_001044385.3:c.*799A>C MANE Select NP_001037850.1:n.*799A>C
NM_152388.4:c.*799A>C NP_689601.2:n.*799A>C
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