Canonical Allele Identifier: CA1321141632
Gene: TMEM237 HGNC NCBI

Linked Data

dbSNP Id: rs1957704188

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201621189T>C , CM000664.2:g.201621189T>C GRCh38
NC_000002.11:g.202485912T>C , CM000664.1:g.202485912T>C GRCh37
NC_000002.10:g.202194157T>C NCBI36
NG_032049.1:g.27341A>G
NG_051007.1:g.2994A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000621467.5:c.*3066A>G ENSP00000480508.2:n.*3066A>G
ENST00000686475.1:n.4233A>G
ENST00000409883.7:c.*3066A>G MANE Select ENSP00000386264.2:n.*3066A>G
ENST00000409444.6:c.*3066A>G ENSP00000387203.2:n.*3066A>G
ENST00000409883.6:c.*3066A>G ENSP00000386264.2:n.*3066A>G
ENST00000495329.1:n.3432A>G
NM_001044385.2:c.*3066A>G NP_001037850.1:n.*3066A>G
NM_152388.3:c.*3066A>G NP_689601.2:n.*3066A>G
NM_001044385.3:c.*3066A>G MANE Select NP_001037850.1:n.*3066A>G
NM_152388.4:c.*3066A>G NP_689601.2:n.*3066A>G