Canonical Allele Identifier: CA2656577979
Gene: TRIOBP HGNC NCBI

Linked Data

gnomAD v4: 22-37768041-A-C
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Genomic Alleles

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

Transcript Alleles

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