Canonical Allele Identifier: CA1321143714
Gene: TMEM237 HGNC NCBI

Linked Data

dbSNP Id: rs1957729089
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201623488C>T , CM000664.2:g.201623488C>T GRCh38
NC_000002.11:g.202488211C>T , CM000664.1:g.202488211C>T GRCh37
NC_000002.10:g.202196456C>T NCBI36
NG_032049.1:g.25042G>A
NG_051007.1:g.695G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000621467.5:c.*767G>A ENSP00000480508.2:n.*767G>A
ENST00000686475.1:n.1934G>A
ENST00000409883.7:c.*767G>A MANE Select ENSP00000386264.2:n.*767G>A
ENST00000409444.6:c.*767G>A ENSP00000387203.2:n.*767G>A
ENST00000409883.6:c.*767G>A ENSP00000386264.2:n.*767G>A
ENST00000495329.1:n.1133G>A
NM_001044385.2:c.*767G>A NP_001037850.1:n.*767G>A
NM_152388.3:c.*767G>A NP_689601.2:n.*767G>A
NM_001044385.3:c.*767G>A MANE Select NP_001037850.1:n.*767G>A
NM_152388.4:c.*767G>A NP_689601.2:n.*767G>A
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