Canonical Allele Identifier: CA889464306
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs1364250553
gnomAD v3: 1-1535294-G-A
gnomAD v4: 1-1535294-G-A
MyVariant Identifiers: chr1:g.1470674G>A (hg19) chr1:g.1535294G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535294G>A , CM000663.2:g.1535294G>A GRCh38
NC_000001.10:g.1470674G>A , CM000663.1:g.1470674G>A GRCh37
NC_000001.9:g.1460537G>A NCBI36
NG_041807.1:g.10067C>T
NG_053035.1:g.28152G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*65C>T MANE Select ENSP00000368007.4:n.*65C>T
ENST00000378733.8:c.*65C>T ENSP00000368007.4:n.*65C>T
ENST00000425828.1:c.*65C>T ENSP00000400311.1:n.*65C>T
NM_001114748.1:c.*65C>T NP_001108220.1:n.*65C>T
NM_001114748.2:c.*65C>T MANE Select NP_001108220.1:n.*65C>T
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