Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50130585A>C , CM000676.2:g.50130585A>C | GRCh38 |
| NC_000014.8:g.50597303A>C , CM000676.1:g.50597303A>C | GRCh37 |
| NC_000014.7:g.49667053A>C | NCBI36 |
| NG_051073.1:g.106109T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216373.10:c.3253T>G MANE Select | ENSP00000216373.5:p.Ser1085Ala | |
| ENST00000216373.9:c.3253T>G | ENSP00000216373.5:p.Ser1085Ala | |
| ENST00000543680.5:c.3154T>G | ENSP00000445328.1:p.Ser1052Ala | |
| NM_006939.2:c.3253T>G | NP_008870.2:p.Ser1085Ala | |
| XM_005268021.1:c.3073T>G | XP_005268078.1:p.Ser1025Ala | |
| XM_011537103.1:c.3214T>G | XP_011535405.1:p.Ser1072Ala | |
| NM_006939.3:c.3253T>G | NP_008870.2:p.Ser1085Ala | |
| NM_006939.4:c.3253T>G MANE Select | NP_008870.2:p.Ser1085Ala |