Canonical Allele Identifier: CA514525069
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs2145821935
MyVariant Identifiers: chr22:g.38109232A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713225A>T , CM000684.2:g.37713225A>T GRCh38
NC_000022.10:g.38109232A>T , CM000684.1:g.38109232A>T GRCh37
NC_000022.9:g.36439178A>T NCBI36
NG_012857.1:g.21238A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.270A>T MANE Select ENSP00000496394.1:p.Ser90=
ENST00000344404.10:c.255-2538A>T ENSP00000340312.6:n.255-2538A>T
ENST00000406386.7:c.270A>T ENSP00000384312.3:p.Ser90=
ENST00000455236.4:c.1227A>T ENSP00000477208.1:n.1227A>T
ENST00000492485.5:n.391-2538A>T
NM_001039141.2:c.270A>T NP_001034230.1:p.Ser90=
NM_001039141.3:c.270A>T MANE Select NP_001034230.1:p.Ser90=