Canonical Allele Identifier: CA520626258
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs1437345515
gnomAD v2: 1-1470631-G-C
gnomAD v3: 1-1535251-G-C
gnomAD v4: 1-1535251-G-C
MyVariant Identifiers: chr1:g.1470631G>C (hg19) chr1:g.1535251G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535251G>C , CM000663.2:g.1535251G>C GRCh38
NC_000001.10:g.1470631G>C , CM000663.1:g.1470631G>C GRCh37
NC_000001.9:g.1460494G>C NCBI36
NG_041807.1:g.10110C>G
NG_053035.1:g.28109G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*108C>G MANE Select ENSP00000368007.4:n.*108C>G
ENST00000378733.8:c.*108C>G ENSP00000368007.4:n.*108C>G
ENST00000425828.1:c.*108C>G ENSP00000400311.1:n.*108C>G
NM_001114748.1:c.*108C>G NP_001108220.1:n.*108C>G
NM_001114748.2:c.*108C>G MANE Select NP_001108220.1:n.*108C>G
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