Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102842702G>C , CM000673.2:g.102842702G>C | GRCh38 |
| NC_000011.9:g.102713433G>C , CM000673.1:g.102713433G>C | GRCh37 |
| NC_000011.8:g.102218643G>C | NCBI36 |
| NG_012100.1:g.5910C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299855.10:c.320C>G MANE Select | ENSP00000299855.5:p.Pro107Arg | |
| ENST00000299855.9:c.320C>G | ENSP00000299855.5:p.Pro107Arg | |
| ENST00000524478.1:c.*162C>G | ENSP00000435255.1:n.*162C>G | |
| NM_002422.3:c.320C>G | NP_002413.1:p.Pro107Arg | |
| NM_002422.4:c.320C>G | NP_002413.1:p.Pro107Arg | |
| NM_002422.5:c.320C>G MANE Select | NP_002413.1:p.Pro107Arg |