Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.72891518T>G , CM000664.2:g.72891518T>G | GRCh38 |
| NC_000002.11:g.73118647T>G , CM000664.1:g.73118647T>G | GRCh37 |
| NC_000002.10:g.72972155T>G | NCBI36 |
| NG_008234.1:g.9136T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000234454.6:c.767T>G MANE Select | ENSP00000234454.5:p.Val256Gly | |
| ENST00000234454.5:c.767T>G | ENSP00000234454.5:p.Val256Gly | |
| ENST00000498749.1:n.712T>G | ||
| NM_003124.4:c.767T>G | NP_003115.1:p.Val256Gly | |
| NM_003124.5:c.767T>G MANE Select | NP_003115.1:p.Val256Gly |