Canonical Allele Identifier: CA6308228
Gene: TREH HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10790256

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118663373C>T , CM000673.2:g.118663373C>T GRCh38
NC_000011.9:g.118534082C>T , CM000673.1:g.118534082C>T GRCh37
NC_000011.8:g.118039292C>T NCBI36
NG_023321.1:g.21300G>A

Transcript Alleles

HGVS Amino-acid change
NM_001301065.1:c.156G>A VV NP_001287994.1:p.Lys52=
NM_007180.2:c.156G>A VV NP_009111.2:p.Lys52=
XM_011542564.1:c.-233-177G>A XP_011540866.1:p.=
ENST00000264029.8:c.156G>A ENSP00000264029.5:p.Lys52=
ENST00000397925.2:c.156G>A ENSP00000381020.2:p.Lys52=
ENST00000527558.1:n.153-177G>A
ENST00000531295.5:n.175G>A
ENST00000613915.4:c.90-177G>A ENSP00000477923.1:p.=