Canonical Allele Identifier: CA324169073
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs532723219
gnomAD v2: 22-38164048-A-G
gnomAD v3: 22-37768041-A-G
gnomAD v4: 22-37768041-A-G
MyVariant Identifiers: chr22:g.38164048A>G (hg19) chr22:g.37768041A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37768041A>G , CM000684.2:g.37768041A>G GRCh38
NC_000022.10:g.38164048A>G , CM000684.1:g.38164048A>G GRCh37
NC_000022.9:g.36493994A>G NCBI36
NG_012857.1:g.76054A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.6473-33A>G MANE Select ENSP00000496394.1:n.6473-33A>G
ENST00000344404.10:c.*5956-33A>G ENSP00000340312.6:n.*5956-33A>G
ENST00000403663.6:c.1334-33A>G ENSP00000386026.2:n.1334-33A>G
ENST00000406386.7:c.6473-33A>G ENSP00000384312.3:n.6473-33A>G
NM_001039141.2:c.6473-33A>G NP_001034230.1:n.6473-33A>G
NM_007032.5:c.1334-33A>G NP_008963.3:n.1334-33A>G
NM_001039141.3:c.6473-33A>G MANE Select NP_001034230.1:n.6473-33A>G
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