Canonical Allele Identifier: CA639394766
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1216239923
gnomAD v2: 22-38109077-A-G
gnomAD v3: 22-37713070-A-G
gnomAD v4: 22-37713070-A-G
MyVariant Identifiers: chr22:g.38109077A>G (hg19) chr22:g.37713070A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37713070A>G , CM000684.2:g.37713070A>G GRCh38
NC_000022.10:g.38109077A>G , CM000684.1:g.38109077A>G GRCh37
NC_000022.9:g.36439023A>G NCBI36
NG_012857.1:g.21083A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.255-140A>G MANE Select ENSP00000496394.1:n.255-140A>G
ENST00000344404.10:c.254+2504A>G ENSP00000340312.6:n.254+2504A>G
ENST00000406386.7:c.255-140A>G ENSP00000384312.3:n.255-140A>G
ENST00000455236.4:c.1212-140A>G ENSP00000477208.1:n.1212-140A>G
ENST00000492485.5:n.390+2504A>G
NM_001039141.2:c.255-140A>G NP_001034230.1:n.255-140A>G
NM_001039141.3:c.255-140A>G MANE Select NP_001034230.1:n.255-140A>G
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