Linked Data
dbSNP Id:
rs1554151707
gnomAD v2:
6-32609618-G-GTGTCGTTA
gnomAD v3:
6-32641841-G-GTGTCGTTA
gnomAD v4:
6-32641841-G-GTGTCGTTA
MyVariant Identifiers:
chr6:g.32609618_32609619insTGTCGTTA (hg19)
chr6:g.32641841_32641842insTGTCGTTA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32641841_32641842insTGTCGTTA , CM000668.2:g.32641841_32641842insTGTCGTTA | GRCh38 |
| NC_000006.11:g.32609618_32609619insTGTCGTTA , CM000668.1:g.32609618_32609619insTGTCGTTA | GRCh37 |
| NC_000006.10:g.32717596_32717597insTGTCGTTA | NCBI36 |
| NG_032876.1:g.9436_9437insTGTCGTTA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343139.11:c.332-131_332-130insTGTCGTTA MANE Select | ENSP00000339398.5:n.332-131_332-130insTGTCGTTA | |
| ENST00000343139.9:c.332-131_332-130insTGTCGTTA | ENSP00000339398.5:n.332-131_332-130insTGTCGTTA | |
| ENST00000374949.2:c.332-131_332-130insTGTCGTTA | ENSP00000364087.2:n.332-131_332-130insTGTCGTTA | |
| ENST00000395363.5:c.332-131_332-130insTGTCGTTA | ENSP00000378767.1:n.332-131_332-130insTGTCGTTA | |
| ENST00000460633.1:n.360-131_360-130insTGTCGTTA | ||
| ENST00000482745.5:c.*1164-131_*1164-130insTGTCGTTA | ENSP00000436546.1:n.*1164-131_*1164-130insTGTCGTTA | |
| ENST00000496318.5:c.332-131_332-130insTGTCGTTA | ENSP00000437302.1:n.332-131_332-130insTGTCGTTA | |
| NM_002122.3:c.332-131_332-130insTGTCGTTA | NP_002113.2:n.332-131_332-130insTGTCGTTA | |
| XM_006715079.2:c.332-131_332-130insTGTCGTTA | XP_006715142.1:n.332-131_332-130insTGTCGTTA | |
| XM_006715079.4:c.332-131_332-130insTGTCGTTA | XP_006715142.1:n.332-131_332-130insTGTCGTTA | |
| XR_001744085.1:n.86+746_86+747insTAACGACA | ||
| NM_002122.5:c.332-131_332-130insTGTCGTTA MANE Select | NP_002113.2:n.332-131_332-130insTGTCGTTA |