Canonical Allele Identifier: CA526697
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs748477956
gnomAD v2: 1-1471147-G-A
gnomAD v3: 1-1535767-G-A
gnomAD v4: 1-1535767-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535767G>A , CM000663.2:g.1535767G>A GRCh38
NC_000001.10:g.1471147G>A , CM000663.1:g.1471147G>A GRCh37
NC_000001.9:g.1461010G>A NCBI36
NG_041807.1:g.9594C>T
NG_053035.1:g.28625G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378733.9:c.195C>T MANE Select ENSP00000368007.4:p.Asp65=
ENST00000378733.8:c.195C>T ENSP00000368007.4:p.Asp65=
ENST00000425828.1:c.195C>T ENSP00000400311.1:p.Asp65=
NM_001114748.1:c.195C>T NP_001108220.1:p.Asp65=
NM_001114748.2:c.195C>T MANE Select NP_001108220.1:p.Asp65=