gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.15891266 (NFE)
Genomes Max Group AF
0.15891266 (NFE)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.233637583A>G , CM000664.2:g.233637583A>G | GRCh38 |
| NC_000002.11:g.234546229A>G , CM000664.1:g.234546229A>G | GRCh37 |
| NC_000002.10:g.234210968A>G | NCBI36 |
| NG_002601.2:g.52840A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344644.10:c.855+206A>G (UGT1A10) MANE Select | ENSP00000343838.5:n.855+206A>G | |
| ENST00000373450.5:c.855+19021A>G (UGT1A8) MANE Select | ENSP00000362549.4:n.855+19021A>G | |
| ENST00000344644.9:c.855+206A>G (UGT1A10) | ENSP00000343838.5:n.855+206A>G | |
| ENST00000373445.1:c.855+206A>G (UGT1A10) | ENSP00000362544.1:n.855+206A>G | |
| ENST00000373450.4:c.855+19021A>G (UGT1A8) | ENSP00000362549.4:n.855+19021A>G | |
| NM_019075.2:c.855+206A>G (UGT1A10) | NP_061948.1:n.855+206A>G | |
| NM_019076.4:c.855+19021A>G (UGT1A8) | NP_061949.3:n.855+19021A>G | |
| NM_019075.4:c.855+206A>G (UGT1A10) MANE Select | NP_061948.1:n.855+206A>G | |
| NM_019076.5:c.855+19021A>G (UGT1A8) MANE Select | NP_061949.3:n.855+19021A>G |