Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101348640C>A , CM000685.2:g.101348640C>A | GRCh38 |
| NC_000023.10:g.100603628C>A , CM000685.1:g.100603628C>A | GRCh37 |
| NC_000023.9:g.100490284C>A | NCBI36 |
| NG_009616.1:g.42585G>T , LRG_128:g.42585G>T | |
| NG_011734.1:g.5330G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372902.4:c.25G>T MANE Select | ENSP00000361993.3:p.Ala9Ser | |
| ENST00000644112.2:c.25G>T | ENSP00000494385.1:p.Ala9Ser | |
| ENST00000645279.1:c.25G>T | ENSP00000494239.1:p.Ala9Ser | |
| ENST00000372902.3:c.25G>T | ENSP00000361993.3:p.Ala9Ser | |
| ENST00000480575.1:n.110G>T | ||
| NM_001145951.1:c.25G>T | NP_001139423.1:p.Ala9Ser | |
| NM_004085.3:c.25G>T | NP_004076.1:p.Ala9Ser | |
| NM_004085.4:c.25G>T MANE Select | NP_004076.1:p.Ala9Ser | |
| NM_001145951.2:c.25G>T | NP_001139423.1:p.Ala9Ser |