Canonical Allele Identifier: CA2662657545
Gene: TMEM237 HGNC NCBI

Linked Data

gnomAD v4: 2-201625965-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201625965G>T , CM000664.2:g.201625965G>T GRCh38
NC_000002.11:g.202490688G>T , CM000664.1:g.202490688G>T GRCh37
NC_000002.10:g.202198933G>T NCBI36
NG_032049.1:g.22565C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000471318.6:n.955+61C>A
ENST00000621467.5:c.1033+61C>A ENSP00000480508.2:n.1033+61C>A
ENST00000686475.1:n.1099+61C>A
ENST00000409883.7:c.1159+61C>A MANE Select ENSP00000386264.2:n.1159+61C>A
ENST00000286196.9:c.*723+61C>A ENSP00000286196.5:n.*723+61C>A
ENST00000409444.6:c.1135+61C>A ENSP00000387203.2:n.1135+61C>A
ENST00000409883.6:c.1159+61C>A ENSP00000386264.2:n.1159+61C>A
ENST00000471318.5:n.387+61C>A
ENST00000495329.1:n.298+61C>A
ENST00000621467.4:c.1135+61C>A ENSP00000480508.1:n.1135+61C>A
NM_001044385.2:c.1159+61C>A NP_001037850.1:n.1159+61C>A
NM_152388.3:c.1135+61C>A NP_689601.2:n.1135+61C>A
NM_001044385.3:c.1159+61C>A MANE Select NP_001037850.1:n.1159+61C>A
NM_152388.4:c.1135+61C>A NP_689601.2:n.1135+61C>A
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