Linked Data
MyVariant Identifiers:
chr17:g.64224148C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.66228030C>T , CM000679.2:g.66228030C>T | GRCh38 |
| NC_000017.10:g.64224148C>T , CM000679.1:g.64224148C>T | GRCh37 |
| NC_000017.9:g.61654610C>T | NCBI36 |
| NG_012045.1:g.6409G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000205948.11:c.231G>A MANE Select | ENSP00000205948.6:p.Leu77= | |
| ENST00000205948.10:c.231G>A | ENSP00000205948.6:p.Leu77= | |
| ENST00000577982.1:c.231G>A | ENSP00000464301.1:p.Leu77= | |
| ENST00000581797.5:c.51G>A | ENSP00000463553.1:p.Leu17= | |
| NM_000042.2:c.231G>A | NP_000033.2:p.Leu77= | |
| NM_000042.3:c.231G>A MANE Select | NP_000033.2:p.Leu77= |