Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119415090G>C , CM000665.2:g.119415090G>C | GRCh38 |
| NC_000003.11:g.119133937G>C , CM000665.1:g.119133937G>C | GRCh37 |
| NC_000003.10:g.120616627G>C | NCBI36 |
| NG_007665.2:g.125718G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.3161G>C MANE Select | ENSP00000264245.4:p.Ser1054Thr | |
| ENST00000264245.8:c.3161G>C | ENSP00000264245.4:p.Ser1054Thr | |
| NM_020754.3:c.3161G>C | NP_065805.2:p.Ser1054Thr | |
| XM_005247671.3:c.3068G>C | XP_005247728.1:p.Ser1023Thr | |
| XM_006713714.2:c.3101G>C | XP_006713777.1:p.Ser1034Thr | |
| XM_006713714.3:c.3101G>C | XP_006713777.1:p.Ser1034Thr | |
| XM_017006955.1:c.2669G>C | XP_016862444.1:p.Ser890Thr | |
| NM_020754.4:c.3161G>C MANE Select | NP_065805.2:p.Ser1054Thr |