Canonical Allele Identifier: CA411487060
Gene: TRIOBP HGNC NCBI

Linked Data

gnomAD v4: 22-37733302-T-C
MyVariant Identifiers: chr22:g.38129309T>C (hg19) chr22:g.37733302T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37733302T>C , CM000684.2:g.37733302T>C GRCh38
NC_000022.10:g.38129309T>C , CM000684.1:g.38129309T>C GRCh37
NC_000022.9:g.36459255T>C NCBI36
NG_012857.1:g.41315T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644935.1:c.3952T>C MANE Select ENSP00000496394.1:p.Ser1318Pro
ENST00000344404.10:c.*3435T>C ENSP00000340312.6:n.*3435T>C
ENST00000406386.7:c.3952T>C ENSP00000384312.3:p.Ser1318Pro
NM_001039141.2:c.3952T>C NP_001034230.1:p.Ser1318Pro
XM_011530646.1:c.512-2943A>G XP_011528948.1:n.512-2943A>G
NM_001039141.3:c.3952T>C MANE Select NP_001034230.1:p.Ser1318Pro
Search 100 bp 5'
Search 100 bp 3'