Linked Data
dbSNP Id:
rs281860437
MyVariant Identifiers:
chr6:g.31239274_31239275insATCCA (hg19)
chr6:g.31271497_31271498insATCCA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31271498_31271499insTCCAA , CM000668.2:g.31271498_31271499insTCCAA | GRCh38 |
| NC_000006.11:g.31239275_31239276insTCCAA , CM000668.1:g.31239275_31239276insTCCAA | GRCh37 |
| NC_000006.10:g.31347254_31347255insTCCAA | NCBI36 |
| NG_029422.2:g.5634_5635insTGGAT |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376228.10:c.343+101_343+102insTGGAT MANE Select | ENSP00000365402.5:n.343+101_343+102insTGG... | |
| ENST00000376228.9:c.343+101_343+102insTGGAT | ENSP00000365402.5:n.343+101_343+102insTGG... | |
| ENST00000376237.8:c.343+101_343+102insTGGAT | ENSP00000365412.4:n.343+101_343+102insTGG... | |
| ENST00000383329.7:c.343+101_343+102insTGGAT | ENSP00000372819.3:n.343+101_343+102insTGG... | |
| ENST00000415537.1:c.341+101_341+102insTGGAT | ||
| ENST00000484378.1:n.463_464insTGGAT | ||
| ENST00000487245.5:n.553_554insTGGAT | ||
| ENST00000495835.1:n.532+101_532+102insTGGAT | ||
| NM_002117.5:c.343+101_343+102insTGGAT | NP_002108.4:n.343+101_343+102insTGGAT | |
| NM_002117.6:c.343+101_343+102insTGGAT MANE Select | NP_002108.4:n.343+101_343+102insTGGAT |