Canonical Allele Identifier: CA2701423439
Gene: TMEM237 HGNC NCBI

Linked Data

dbSNP Id: rs2105894785
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201621150A>G , CM000664.2:g.201621150A>G GRCh38
NC_000002.11:g.202485873A>G , CM000664.1:g.202485873A>G GRCh37
NC_000002.10:g.202194118A>G NCBI36
NG_032049.1:g.27380T>C
NG_051007.1:g.3033T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000621467.5:c.*3105T>C ENSP00000480508.2:n.*3105T>C
ENST00000686475.1:n.4272T>C
ENST00000409883.7:c.*3105T>C MANE Select ENSP00000386264.2:n.*3105T>C
ENST00000409444.6:c.*3105T>C ENSP00000387203.2:n.*3105T>C
ENST00000409883.6:c.*3105T>C ENSP00000386264.2:n.*3105T>C
ENST00000495329.1:n.3471T>C
NM_001044385.2:c.*3105T>C NP_001037850.1:n.*3105T>C
NM_152388.3:c.*3105T>C NP_689601.2:n.*3105T>C
NM_001044385.3:c.*3105T>C MANE Select NP_001037850.1:n.*3105T>C
NM_152388.4:c.*3105T>C NP_689601.2:n.*3105T>C
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