Canonical Allele Identifier: CA10225071
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs780373703
ExAC: 22:38164031 G / T
gnomAD v2: 22-38164031-G-T
gnomAD v4: 22-37768024-G-T
MyVariant Identifiers: chr22:g.38164031G>T (hg19) chr22:g.37768024G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37768024G>T , CM000684.2:g.37768024G>T GRCh38
NC_000022.10:g.38164031G>T , CM000684.1:g.38164031G>T GRCh37
NC_000022.9:g.36493977G>T NCBI36
NG_012857.1:g.76037G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.6473-50G>T MANE Select ENSP00000496394.1:n.6473-50G>T
ENST00000344404.10:c.*5956-50G>T ENSP00000340312.6:n.*5956-50G>T
ENST00000403663.6:c.1334-50G>T ENSP00000386026.2:n.1334-50G>T
ENST00000406386.7:c.6473-50G>T ENSP00000384312.3:n.6473-50G>T
NM_001039141.2:c.6473-50G>T NP_001034230.1:n.6473-50G>T
NM_007032.5:c.1334-50G>T NP_008963.3:n.1334-50G>T
NM_001039141.3:c.6473-50G>T MANE Select NP_001034230.1:n.6473-50G>T
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