Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.178014460C>G , CM000664.2:g.178014460C>G | GRCh38 |
| NC_000002.11:g.178879187C>G , CM000664.1:g.178879187C>G | GRCh37 |
| NC_000002.10:g.178587433C>G | NCBI36 |
| NG_012168.1:g.98880G>C | |
| NG_012168.2:g.98880G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286063.11:c.913G>C MANE Select | ENSP00000286063.5:p.Asp305His | |
| ENST00000286063.10:c.913G>C | ENSP00000286063.5:p.Asp305His | |
| ENST00000358450.8:c.163G>C | ENSP00000351232.4:p.Asp55His | |
| NM_001077197.1:c.163G>C | NP_001070665.1:p.Asp55His | |
| NM_016953.3:c.913G>C | NP_058649.3:p.Asp305His | |
| NM_016953.4:c.913G>C MANE Select | NP_058649.3:p.Asp305His | |
| NM_001077197.2:c.163G>C | NP_001070665.1:p.Asp55His |