Canonical Allele Identifier: CA1149191469
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs1570368827
gnomAD v4: 1-1535316-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535316A>G , CM000663.2:g.1535316A>G GRCh38
NC_000001.10:g.1470696A>G , CM000663.1:g.1470696A>G GRCh37
NC_000001.9:g.1460559A>G NCBI36
NG_041807.1:g.10045T>C
NG_053035.1:g.28174A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*43T>C MANE Select ENSP00000368007.4:n.*43T>C
ENST00000378733.8:c.*43T>C ENSP00000368007.4:n.*43T>C
ENST00000425828.1:c.*43T>C ENSP00000400311.1:n.*43T>C
NM_001114748.1:c.*43T>C NP_001108220.1:n.*43T>C
NM_001114748.2:c.*43T>C MANE Select NP_001108220.1:n.*43T>C
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