Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.50193021A>C , CM000685.2:g.50193021A>C | GRCh38 |
| NC_000023.10:g.49957672A>C , CM000685.1:g.49957672A>C | GRCh37 |
| NC_000023.9:g.49844412A>C | NCBI36 |
| NG_012552.1:g.12993T>G | |
| NG_012552.2:g.12993T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358526.7:c.1692T>G MANE Select | ENSP00000351327.2:p.Asp564Glu | |
| ENST00000358526.6:c.1692T>G | ENSP00000351327.2:p.Asp564Glu | |
| ENST00000376064.7:c.1665T>G | ENSP00000365232.3:p.Asp555Glu | |
| ENST00000448865.5:c.543T>G | ENSP00000402403.1:p.Asn181Lys | |
| ENST00000481402.5:n.1804T>G | ||
| NM_003886.2:c.1692T>G | NP_003877.2:p.Asp564Glu | |
| NM_139289.1:c.1665T>G | NP_647450.1:p.Asp555Glu | |
| NM_003886.3:c.1692T>G MANE Select | NP_003877.2:p.Asp564Glu | |
| NM_139289.2:c.1665T>G | NP_647450.1:p.Asp555Glu |