Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99420579T>C , CM000666.2:g.99420579T>C | GRCh38 |
| NC_000004.11:g.100341736T>C , CM000666.1:g.100341736T>C | GRCh37 |
| NC_000004.10:g.100560759T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000437033.7:c.779A>G MANE Select | ENSP00000414254.2:p.Asn260Ser | |
| ENST00000209665.8:c.815A>G | ENSP00000209665.4:p.Asn272Ser | |
| ENST00000437033.6:c.779A>G | ENSP00000414254.2:p.Asn260Ser | |
| ENST00000476959.5:c.839A>G | ENSP00000420269.1:p.Asn280Ser | |
| ENST00000482593.5:c.608A>G | ENSP00000420613.1:p.Asn203Ser | |
| NM_000673.4:c.815A>G | NP_000664.2:p.Asn272Ser | |
| NM_001166504.1:c.839A>G | NP_001159976.1:p.Asn280Ser | |
| NM_000673.7:c.779A>G MANE Select | NP_000664.3:p.Asn260Ser | |
| NM_001166504.2:c.839A>G | NP_001159976.1:p.Asn280Ser |