Canonical Allele Identifier: CA10223401
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs745592830
ExAC: 22:38111982 G / T
gnomAD v2: 22-38111982-G-T
gnomAD v3: 22-37715975-G-T
gnomAD v4: 22-37715975-G-T
MyVariant Identifiers: chr22:g.38111982G>T (hg19) chr22:g.37715975G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37715975G>T , CM000684.2:g.37715975G>T GRCh38
NC_000022.10:g.38111982G>T , CM000684.1:g.38111982G>T GRCh37
NC_000022.9:g.36441928G>T NCBI36
NG_012857.1:g.23988G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.628+41G>T MANE Select ENSP00000496394.1:n.628+41G>T
ENST00000344404.10:c.*111+41G>T ENSP00000340312.6:n.*111+41G>T
ENST00000406386.7:c.628+41G>T ENSP00000384312.3:n.628+41G>T
ENST00000455236.4:c.1585+41G>T ENSP00000477208.1:n.1585+41G>T
ENST00000492485.5:n.562+41G>T
NM_001039141.2:c.628+41G>T NP_001034230.1:n.628+41G>T
NM_001039141.3:c.628+41G>T MANE Select NP_001034230.1:n.628+41G>T
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