Canonical Allele Identifier: CA10586814
Gene: TMEM237 HGNC NCBI

Linked Data

ClinVar Variation Id: 257312
ClinVar RCV Id: RCV000251323
dbSNP Id: rs886038402
gnomAD v4: 2-201643404-G-C
MyVariant Identifiers: chr2:g.202508127G>C (hg19) chr2:g.201643404G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201643404G>C , CM000664.2:g.201643404G>C GRCh38
NC_000002.11:g.202508127G>C , CM000664.1:g.202508127G>C GRCh37
NC_000002.10:g.202216372G>C NCBI36
NG_012654.1:g.60291C>G
NG_032049.1:g.5126C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409883.7:c.-4C>G MANE Select ENSP00000386264.2:n.-4C>G
ENST00000286196.9:c.-78C>G ENSP00000286196.5:n.-78C>G
ENST00000409883.6:c.-4C>G ENSP00000386264.2:n.-4C>G
ENST00000432684.6:c.-4C>G ENSP00000413230.2:n.-4C>G
ENST00000489550.5:n.15C>G
NM_001044385.2:c.-4C>G NP_001037850.1:n.-4C>G
NM_001044385.3:c.-4C>G MANE Select NP_001037850.1:n.-4C>G
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