Canonical Allele Identifier: CA1149191488
Gene: TMEM240 HGNC NCBI

Linked Data

dbSNP Id: rs1642195598
gnomAD v4: 1-1535329-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1535329C>T , CM000663.2:g.1535329C>T GRCh38
NC_000001.10:g.1470709C>T , CM000663.1:g.1470709C>T GRCh37
NC_000001.9:g.1460572C>T NCBI36
NG_041807.1:g.10032G>A
NG_053035.1:g.28187C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378733.9:c.*30G>A MANE Select ENSP00000368007.4:n.*30G>A
ENST00000378733.8:c.*30G>A ENSP00000368007.4:n.*30G>A
ENST00000425828.1:c.*30G>A ENSP00000400311.1:n.*30G>A
NM_001114748.1:c.*30G>A NP_001108220.1:n.*30G>A
NM_001114748.2:c.*30G>A MANE Select NP_001108220.1:n.*30G>A
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