Canonical Allele Identifier: CA752905454
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1171753020
gnomAD v4: 22-37713067-C-T
MyVariant Identifiers: chr22:g.38109074C>T (hg19) chr22:g.37713067C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713067C>T , CM000684.2:g.37713067C>T GRCh38
NC_000022.10:g.38109074C>T , CM000684.1:g.38109074C>T GRCh37
NC_000022.9:g.36439020C>T NCBI36
NG_012857.1:g.21080C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.255-143C>T MANE Select ENSP00000496394.1:n.255-143C>T
ENST00000344404.10:c.254+2501C>T ENSP00000340312.6:n.254+2501C>T
ENST00000406386.7:c.255-143C>T ENSP00000384312.3:n.255-143C>T
ENST00000455236.4:c.1212-143C>T ENSP00000477208.1:n.1212-143C>T
ENST00000492485.5:n.390+2501C>T
NM_001039141.2:c.255-143C>T NP_001034230.1:n.255-143C>T
NM_001039141.3:c.255-143C>T MANE Select NP_001034230.1:n.255-143C>T
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