Canonical Allele Identifier: CA337865927
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs770406796
gnomAD v4: 1-1535431-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535431C>G , CM000663.2:g.1535431C>G GRCh38
NC_000001.10:g.1470811C>G , CM000663.1:g.1470811C>G GRCh37
NC_000001.9:g.1460674C>G NCBI36
NG_041807.1:g.9930G>C
NG_053035.1:g.28289C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.450G>C MANE Select ENSP00000368007.4:p.Glu150Asp
ENST00000378733.8:c.450G>C ENSP00000368007.4:p.Glu150Asp
ENST00000425828.1:c.450G>C ENSP00000400311.1:p.Glu150Asp
NM_001114748.1:c.450G>C NP_001108220.1:p.Glu150Asp
NM_001114748.2:c.450G>C MANE Select NP_001108220.1:p.Glu150Asp