Canonical Allele Identifier: CA10225085
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs751101904
ExAC: 22:38164143 A / T
gnomAD v2: 22-38164143-A-T
gnomAD v4: 22-37768136-A-T
MyVariant Identifiers: chr22:g.38164143A>T (hg19) chr22:g.37768136A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37768136A>T , CM000684.2:g.37768136A>T GRCh38
NC_000022.10:g.38164143A>T , CM000684.1:g.38164143A>T GRCh37
NC_000022.9:g.36494089A>T NCBI36
NG_012857.1:g.76149A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.6535A>T MANE Select ENSP00000496394.1:p.Ser2179Cys
ENST00000344404.10:c.*6018A>T ENSP00000340312.6:n.*6018A>T
ENST00000403663.6:c.1396A>T ENSP00000386026.2:p.Ser466Cys
ENST00000406386.7:c.6535A>T ENSP00000384312.3:p.Ser2179Cys
NM_001039141.2:c.6535A>T NP_001034230.1:p.Ser2179Cys
NM_007032.5:c.1396A>T NP_008963.3:p.Ser466Cys
NM_001039141.3:c.6535A>T MANE Select NP_001034230.1:p.Ser2179Cys
Search 100 bp 5'
Search 100 bp 3'