Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56983391C>A , CM000678.2:g.56983391C>A | GRCh38 |
| NC_000016.9:g.57017303C>A , CM000678.1:g.57017303C>A | GRCh37 |
| NC_000016.8:g.55574804C>A | NCBI36 |
| NG_008952.1:g.26469C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000200676.8:c.1387C>A MANE Select | ENSP00000200676.3:p.Pro463Thr | |
| ENST00000650358.1:n.1785C>A | ||
| ENST00000200676.7:c.1387C>A | ENSP00000200676.3:p.Pro463Thr | |
| ENST00000379780.6:c.1207C>A | ENSP00000369106.2:p.Pro403Thr | |
| ENST00000566128.1:c.1192C>A | ENSP00000456276.1:p.Pro398Thr | |
| NM_000078.2:c.1387C>A | NP_000069.2:p.Pro463Thr | |
| NM_001286085.1:c.1207C>A | NP_001273014.1:p.Pro403Thr | |
| NM_000078.3:c.1387C>A MANE Select | NP_000069.2:p.Pro463Thr | |
| NM_001286085.2:c.1207C>A | NP_001273014.1:p.Pro403Thr |