Linked Data
gnomAD v2:
2-234546073-T-TAAAAAAAA
MyVariant Identifiers:
chr2:g.234546074_234546075insAAAAAAAA (hg19)
chr2:g.233637428_233637429insAAAAAAAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.233637433_233637434insAAAAAAAA , CM000664.2:g.233637433_233637434insAAAAAAAA | GRCh38 |
| NC_000002.11:g.234546079_234546080insAAAAAAAA , CM000664.1:g.234546079_234546080insAAAAAAAA | GRCh37 |
| NC_000002.10:g.234210818_234210819insAAAAAAAA | NCBI36 |
| NG_002601.2:g.52690_52691insAAAAAAAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344644.10:c.855+56_855+57insAAAAAAAA (UGT1A10) MANE Select | ENSP00000343838.5:n.855+56_855+57insAAAAAAAA | |
| ENST00000373450.5:c.855+18871_855+18872insAAAAAAAA (UGT1A8) MANE Select | ENSP00000362549.4:n.855+18871_855+18872insAAAAAAAA | |
| ENST00000344644.9:c.855+56_855+57insAAAAAAAA (UGT1A10) | ENSP00000343838.5:n.855+56_855+57insAAAAAAAA | |
| ENST00000373445.1:c.855+56_855+57insAAAAAAAA (UGT1A10) | ENSP00000362544.1:n.855+56_855+57insAAAAAAAA | |
| ENST00000373450.4:c.855+18871_855+18872insAAAAAAAA (UGT1A8) | ENSP00000362549.4:n.855+18871_855+18872insAAAAAAAA | |
| NM_019075.2:c.855+56_855+57insAAAAAAAA (UGT1A10) | NP_061948.1:n.855+56_855+57insAAAAAAAA | |
| NM_019076.4:c.855+18871_855+18872insAAAAAAAA (UGT1A8) | NP_061949.3:n.855+18871_855+18872insAAAAAAAA | |
| NM_019075.4:c.855+56_855+57insAAAAAAAA (UGT1A10) MANE Select | NP_061948.1:n.855+56_855+57insAAAAAAAA | |
| NM_019076.5:c.855+18871_855+18872insAAAAAAAA (UGT1A8) MANE Select | NP_061949.3:n.855+18871_855+18872insAAAAAAAA |