Canonical Allele Identifier: CA411489123
Gene: TRIOBP HGNC NCBI

Linked Data

dbSNP Id: rs775714830
gnomAD v4: 22-37734476-G-C
MyVariant Identifiers: chr22:g.38130483G>C (hg19) chr22:g.37734476G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.37734476G>C , CM000684.2:g.37734476G>C GRCh38
NC_000022.10:g.38130483G>C , CM000684.1:g.38130483G>C GRCh37
NC_000022.9:g.36460429G>C NCBI36
NG_012857.1:g.42489G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644935.1:c.4140G>C MANE Select ENSP00000496394.1:p.Glu1380Asp
ENST00000344404.10:c.*3623G>C ENSP00000340312.6:n.*3623G>C
ENST00000406386.7:c.4140G>C ENSP00000384312.3:p.Glu1380Asp
NM_001039141.2:c.4140G>C NP_001034230.1:p.Glu1380Asp
XM_011530646.1:c.512-4117C>G XP_011528948.1:n.512-4117C>G
NM_001039141.3:c.4140G>C MANE Select NP_001034230.1:p.Glu1380Asp
Search 100 bp 5'
Search 100 bp 3'