Canonical Allele Identifier: CA337867238
Gene: TMEM240 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.1471152A>G (hg19) chr1:g.1535772A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535772A>G , CM000663.2:g.1535772A>G GRCh38
NC_000001.10:g.1471152A>G , CM000663.1:g.1471152A>G GRCh37
NC_000001.9:g.1461015A>G NCBI36
NG_041807.1:g.9589T>C
NG_053035.1:g.28630A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378733.9:c.190T>C MANE Select ENSP00000368007.4:p.Tyr64His
ENST00000378733.8:c.190T>C ENSP00000368007.4:p.Tyr64His
ENST00000425828.1:c.190T>C ENSP00000400311.1:p.Tyr64His
NM_001114748.1:c.190T>C NP_001108220.1:p.Tyr64His
NM_001114748.2:c.190T>C MANE Select NP_001108220.1:p.Tyr64His
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