Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372404T>C , CM000679.2:g.44372404T>C | GRCh38 |
| NC_000017.10:g.42449772T>C , CM000679.1:g.42449772T>C | GRCh37 |
| NC_000017.9:g.39805298T>C | NCBI36 |
| NG_008331.1:g.22102A>G , LRG_479:g.22102A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.3080A>G MANE Select | ENSP00000262407.5:p.Asn1027Ser | |
| ENST00000648408.1:c.2394A>G | ||
| ENST00000262407.5:c.3080A>G | ENSP00000262407.5:p.Asn1027Ser | |
| ENST00000587295.5:c.273A>G | ||
| ENST00000588098.1:c.57A>G | ||
| NM_000419.3:c.3080A>G , LRG_479t1:c.3080A>G | NP_000410.2:p.Asn1027Ser | |
| XM_011524749.1:c.2978A>G | XP_011523051.1:p.Asn993Ser | |
| XM_011524750.1:c.2963A>G | XP_011523052.1:p.Asn988Ser | |
| NM_000419.4:c.3080A>G | NP_000410.2:p.Asn1027Ser | |
| NM_000419.5:c.3080A>G MANE Select | NP_000410.2:p.Asn1027Ser |