Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.99844322G>T , CM000672.2:g.99844322G>T | GRCh38 |
| NC_000010.10:g.101604079G>T , CM000672.1:g.101604079G>T | GRCh37 |
| NC_000010.9:g.101594069G>T | NCBI36 |
| NG_011798.1:g.66617G>T | |
| NG_011798.2:g.66725G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647814.1:c.3844G>T MANE Select | ENSP00000497274.1:p.Ala1282Ser | |
| ENST00000649459.1:n.192G>T | ||
| ENST00000370449.8:c.3844G>T | ENSP00000359478.4:p.Ala1282Ser | |
| NM_000392.4:c.3844G>T | NP_000383.1:p.Ala1282Ser | |
| XM_006717630.2:c.3148G>T | XP_006717693.1:p.Ala1050Ser | |
| XR_945604.1:n.4033G>T | ||
| XR_945605.1:n.3908G>T | ||
| NM_000392.5:c.3844G>T MANE Select | NP_000383.2:p.Ala1282Ser | |
| XM_006717630.3:c.3148G>T | XP_006717693.1:p.Ala1050Ser | |
| XR_945604.3:n.4087G>T | ||
| XR_945605.3:n.3960G>T |