Linked Data
gnomAD v4:
8-10622527-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.10622527A>G , CM000670.2:g.10622527A>G | GRCh38 |
| NC_000008.10:g.10480037A>G , CM000670.1:g.10480037A>G | GRCh37 |
| NC_000008.9:g.10517447A>G | NCBI36 |
| NG_028035.1:g.37581T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382483.4:c.609+66T>C MANE Select | ENSP00000371923.3:n.609+66T>C | |
| ENST00000329335.3:n.859+66T>C | ||
| ENST00000382483.3:c.609+66T>C | ENSP00000371923.3:n.609+66T>C | |
| NM_178857.5:c.609+66T>C | NP_849188.4:n.609+66T>C | |
| NM_178857.6:c.609+66T>C MANE Select | NP_849188.4:n.609+66T>C |