Canonical Allele Identifier: CA337866859
Gene: TMEM240 HGNC NCBI

Linked Data

gnomAD v4: 1-1535696-T-C
MyVariant Identifiers: chr1:g.1471076T>C (hg19) chr1:g.1535696T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535696T>C , CM000663.2:g.1535696T>C GRCh38
NC_000001.10:g.1471076T>C , CM000663.1:g.1471076T>C GRCh37
NC_000001.9:g.1460939T>C NCBI36
NG_041807.1:g.9665A>G
NG_053035.1:g.28554T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.266A>G MANE Select ENSP00000368007.4:p.Asp89Gly
ENST00000378733.8:c.266A>G ENSP00000368007.4:p.Asp89Gly
ENST00000425828.1:c.266A>G ENSP00000400311.1:p.Asp89Gly
NM_001114748.1:c.266A>G NP_001108220.1:p.Asp89Gly
NM_001114748.2:c.266A>G MANE Select NP_001108220.1:p.Asp89Gly
Search 100 bp 5'
Search 100 bp 3'