Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6224713A>C , CM000668.2:g.6224713A>C | GRCh38 |
| NC_000006.11:g.6224946A>C , CM000668.1:g.6224946A>C | GRCh37 |
| NC_000006.10:g.6169945A>C | NCBI36 |
| NG_008107.1:g.100979T>G , LRG_549:g.100979T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264870.8:c.946T>G MANE Select | ENSP00000264870.3:p.Trp316Gly | |
| ENST00000264870.7:c.946T>G | ENSP00000264870.3:p.Trp316Gly | |
| ENST00000445223.1:c.96T>G | ||
| NM_000129.3:c.946T>G , LRG_549t1:c.946T>G | NP_000120.2:p.Trp316Gly | |
| XM_006715010.2:c.946T>G | XP_006715073.1:p.Trp316Gly | |
| XM_011514342.1:c.1108T>G | XP_011512644.1:p.Trp370Gly | |
| NM_000129.4:c.946T>G MANE Select | NP_000120.2:p.Trp316Gly |