Canonical Allele Identifier: CA494484830
Gene: TUFM HGNC NCBI

Linked Data

ClinVar Variation Id: 1539050
ClinVar RCV Id: RCV002162298
dbSNP Id: rs2152147557
MyVariant Identifiers: chr16:g.28856650A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.28845329A>G , CM000678.2:g.28845329A>G GRCh38
NC_000016.9:g.28856650A>G , CM000678.1:g.28856650A>G GRCh37
NC_000016.8:g.28764151A>G NCBI36
NG_008964.1:g.6080T>C
NG_029706.2:g.3730A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313511.8:c.399T>C MANE Select ENSP00000322439.3:p.His133=
ENST00000313511.7:c.399T>C ENSP00000322439.3:p.His133=
ENST00000565012.1:c.248-274T>C ENSP00000455007.1:n.248-274T>C
NM_003321.4:c.399T>C NP_003312.3:p.His133=
XM_011545928.1:c.399T>C XP_011544230.1:p.His133=
NM_001365360.1:c.399T>C NP_001352289.1:p.His133=
NM_003321.5:c.399T>C MANE Select NP_003312.3:p.His133=
NM_001365360.2:c.399T>C NP_001352289.1:p.His133=