Canonical Allele Identifier: CA526703
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs762978280
ExAC: 1:1471202 A / C
gnomAD v4: 1-1535822-A-C
MyVariant Identifiers: chr1:g.1471202A>C (hg19) chr1:g.1535822A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535822A>C , CM000663.2:g.1535822A>C GRCh38
NC_000001.10:g.1471202A>C , CM000663.1:g.1471202A>C GRCh37
NC_000001.9:g.1461065A>C NCBI36
NG_041807.1:g.9539T>G
NG_053035.1:g.28680A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.165-25T>G MANE Select ENSP00000368007.4:n.165-25T>G
ENST00000378733.8:c.165-25T>G ENSP00000368007.4:n.165-25T>G
ENST00000425828.1:c.165-25T>G ENSP00000400311.1:n.165-25T>G
NM_001114748.1:c.165-25T>G NP_001108220.1:n.165-25T>G
NM_001114748.2:c.165-25T>G MANE Select NP_001108220.1:n.165-25T>G
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