Canonical Allele Identifier: CA520626266
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs1190218399
gnomAD v2: 1-1470713-G-T
gnomAD v4: 1-1535333-G-T
MyVariant Identifiers: chr1:g.1470713G>T (hg19) chr1:g.1535333G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535333G>T , CM000663.2:g.1535333G>T GRCh38
NC_000001.10:g.1470713G>T , CM000663.1:g.1470713G>T GRCh37
NC_000001.9:g.1460576G>T NCBI36
NG_041807.1:g.10028C>A
NG_053035.1:g.28191G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*26C>A MANE Select ENSP00000368007.4:n.*26C>A
ENST00000378733.8:c.*26C>A ENSP00000368007.4:n.*26C>A
ENST00000425828.1:c.*26C>A ENSP00000400311.1:n.*26C>A
NM_001114748.1:c.*26C>A NP_001108220.1:n.*26C>A
NM_001114748.2:c.*26C>A MANE Select NP_001108220.1:n.*26C>A
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