Linked Data
gnomAD v4:
17-66228072-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.66228072C>A , CM000679.2:g.66228072C>A | GRCh38 |
| NC_000017.10:g.64224190C>A , CM000679.1:g.64224190C>A | GRCh37 |
| NC_000017.9:g.61654652C>A | NCBI36 |
| NG_012045.1:g.6367G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000205948.11:c.189G>T MANE Select | ENSP00000205948.6:p.Lys63Asn | |
| ENST00000205948.10:c.189G>T | ENSP00000205948.6:p.Lys63Asn | |
| ENST00000577982.1:c.189G>T | ENSP00000464301.1:p.Lys63Asn | |
| ENST00000581797.5:c.9G>T | ENSP00000463553.1:p.Lys3Asn | |
| NM_000042.2:c.189G>T | NP_000033.2:p.Lys63Asn | |
| NM_000042.3:c.189G>T MANE Select | NP_000033.2:p.Lys63Asn |