Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6145665A>C , CM000668.2:g.6145665A>C | GRCh38 |
| NC_000006.11:g.6145898A>C , CM000668.1:g.6145898A>C | GRCh37 |
| NC_000006.10:g.6090897A>C | NCBI36 |
| NG_008107.1:g.180027T>G , LRG_549:g.180027T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264870.8:c.2153T>G MANE Select | ENSP00000264870.3:p.Val718Gly | |
| ENST00000264870.7:c.2153T>G | ENSP00000264870.3:p.Val718Gly | |
| NM_000129.3:c.2153T>G , LRG_549t1:c.2153T>G | NP_000120.2:p.Val718Gly | |
| XM_006715010.2:c.2153T>G | XP_006715073.1:p.Val718Gly | |
| XM_011514342.1:c.2315T>G | XP_011512644.1:p.Val772Gly | |
| NM_000129.4:c.2153T>G MANE Select | NP_000120.2:p.Val718Gly |