Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372416A>G , CM000679.2:g.44372416A>G | GRCh38 |
| NC_000017.10:g.42449784A>G , CM000679.1:g.42449784A>G | GRCh37 |
| NC_000017.9:g.39805310A>G | NCBI36 |
| NG_008331.1:g.22090T>C , LRG_479:g.22090T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.3068T>C MANE Select | ENSP00000262407.5:p.Phe1023Ser | |
| ENST00000648408.1:c.2382T>C | ||
| ENST00000262407.5:c.3068T>C | ENSP00000262407.5:p.Phe1023Ser | |
| ENST00000587295.5:c.261T>C | ||
| ENST00000588098.1:c.45T>C | ||
| NM_000419.3:c.3068T>C , LRG_479t1:c.3068T>C | NP_000410.2:p.Phe1023Ser | |
| XM_011524749.1:c.2966T>C | XP_011523051.1:p.Phe989Ser | |
| XM_011524750.1:c.2951T>C | XP_011523052.1:p.Phe984Ser | |
| NM_000419.4:c.3068T>C | NP_000410.2:p.Phe1023Ser | |
| NM_000419.5:c.3068T>C MANE Select | NP_000410.2:p.Phe1023Ser |