Canonical Allele Identifier: CA411487299
Gene: TRIOBP HGNC NCBI

Linked Data

gnomAD v4: 22-37733357-G-C
MyVariant Identifiers: chr22:g.38129364G>C (hg19) chr22:g.37733357G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733357G>C , CM000684.2:g.37733357G>C GRCh38
NC_000022.10:g.38129364G>C , CM000684.1:g.38129364G>C GRCh37
NC_000022.9:g.36459310G>C NCBI36
NG_012857.1:g.41370G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.4007G>C MANE Select ENSP00000496394.1:p.Ser1336Thr
ENST00000344404.10:c.*3490G>C ENSP00000340312.6:n.*3490G>C
ENST00000406386.7:c.4007G>C ENSP00000384312.3:p.Ser1336Thr
NM_001039141.2:c.4007G>C NP_001034230.1:p.Ser1336Thr
XM_011530646.1:c.512-2998C>G XP_011528948.1:n.512-2998C>G
NM_001039141.3:c.4007G>C MANE Select NP_001034230.1:p.Ser1336Thr
Search 100 bp 5'
Search 100 bp 3'