Canonical Allele Identifier: CA752931267
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1222292910
MyVariant Identifiers: chr22:g.37733148C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733148C>T , CM000684.2:g.37733148C>T GRCh38
NC_000022.10:g.38129155C>T , CM000684.1:g.38129155C>T GRCh37
NC_000022.9:g.36459101C>T NCBI36
NG_012857.1:g.41161C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.3948-150C>T MANE Select ENSP00000496394.1:n.3948-150C>T
ENST00000344404.10:c.*3431-150C>T ENSP00000340312.6:n.*3431-150C>T
ENST00000406386.7:c.3948-150C>T ENSP00000384312.3:n.3948-150C>T
NM_001039141.2:c.3948-150C>T NP_001034230.1:n.3948-150C>T
XM_011530646.1:c.512-2789G>A XP_011528948.1:n.512-2789G>A
NM_001039141.3:c.3948-150C>T MANE Select NP_001034230.1:n.3948-150C>T