Canonical Allele Identifier: CA639197021
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs1253461242
gnomAD v2: 22-38130378-C-T
gnomAD v4: 22-37734371-C-T
MyVariant Identifiers: chr22:g.38130378C>T (hg19) chr22:g.37734371C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37734371C>T , CM000684.2:g.37734371C>T GRCh38
NC_000022.10:g.38130378C>T , CM000684.1:g.38130378C>T GRCh37
NC_000022.9:g.36460324C>T NCBI36
NG_012857.1:g.42384C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.4063-28C>T MANE Select ENSP00000496394.1:n.4063-28C>T
ENST00000344404.10:c.*3546-28C>T ENSP00000340312.6:n.*3546-28C>T
ENST00000406386.7:c.4063-28C>T ENSP00000384312.3:n.4063-28C>T
NM_001039141.2:c.4063-28C>T NP_001034230.1:n.4063-28C>T
XM_011530646.1:c.512-4012G>A XP_011528948.1:n.512-4012G>A
NM_001039141.3:c.4063-28C>T MANE Select NP_001034230.1:n.4063-28C>T
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