Canonical Allele Identifier: CA337866760
Gene: TMEM240 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.1471052C>G (hg19) chr1:g.1535672C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535672C>G , CM000663.2:g.1535672C>G GRCh38
NC_000001.10:g.1471052C>G , CM000663.1:g.1471052C>G GRCh37
NC_000001.9:g.1460915C>G NCBI36
NG_041807.1:g.9689G>C
NG_053035.1:g.28530C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378733.9:c.290G>C MANE Select ENSP00000368007.4:p.Gly97Ala
ENST00000378733.8:c.290G>C ENSP00000368007.4:p.Gly97Ala
ENST00000425828.1:c.290G>C ENSP00000400311.1:p.Gly97Ala
NM_001114748.1:c.290G>C NP_001108220.1:p.Gly97Ala
NM_001114748.2:c.290G>C MANE Select NP_001108220.1:p.Gly97Ala
Search 100 bp 5'
Search 100 bp 3'