Linked Data
gnomAD v2:
6-151847669-T-TTTA
gnomAD v3:
6-151526534-T-TTTA
gnomAD v4:
6-151526534-T-TTTA
MyVariant Identifiers:
chr6:g.151847670_151847671delinsTTAGA (hg19)
chr6:g.151526535_151526536delinsTTAGA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151526534_151526535insTTA , CM000668.2:g.151526534_151526535insTTA | GRCh38 |
| NC_000006.11:g.151847669_151847670insTTA , CM000668.1:g.151847669_151847670insTTA | GRCh37 |
| NC_000006.10:g.151889362_151889363insTTA | NCBI36 |
| NG_021198.1:g.37495_37496insTTA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239374.8:c.58-9784_58-9783insTTA MANE Select | ENSP00000239374.6:n.58-9784_58-9783insTTA | |
| ENST00000239374.7:c.58-9784_58-9783insTTA | ENSP00000239374.6:n.58-9784_58-9783insTTA | |
| NM_025059.3:c.58-9784_58-9783insTTA | NP_079335.2:n.58-9784_58-9783insTTA | |
| NM_025059.4:c.58-9784_58-9783insTTA MANE Select | NP_079335.2:n.58-9784_58-9783insTTA |