Canonical Allele Identifier: CA2725235212
Gene: TREH HGNC NCBI

Linked Data

dbSNP Id: rs2137259890

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118659702G>A , CM000673.2:g.118659702G>A GRCh38
NC_000011.9:g.118530411G>A , CM000673.1:g.118530411G>A GRCh37
NC_000011.8:g.118035621G>A NCBI36
NG_023321.1:g.24971C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264029.9:c.1320+45C>T MANE Select ENSP00000264029.5:n.1320+45C>T
ENST00000264029.8:c.1320+45C>T ENSP00000264029.5:n.1320+45C>T
ENST00000397925.2:c.1227+45C>T ENSP00000381020.2:n.1227+45C>T
ENST00000613915.4:c.*1097+45C>T ENSP00000477923.1:n.*1097+45C>T
NM_001301065.1:c.1227+45C>T NP_001287994.1:n.1227+45C>T
NM_007180.2:c.1320+45C>T NP_009111.2:n.1320+45C>T
XM_011542564.1:c.897+45C>T XP_011540866.1:n.897+45C>T
NM_001301065.2:c.1227+45C>T NP_001287994.1:n.1227+45C>T
NM_007180.3:c.1320+45C>T MANE Select NP_009111.2:n.1320+45C>T