Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56983388A>T , CM000678.2:g.56983388A>T | GRCh38 |
| NC_000016.9:g.57017300A>T , CM000678.1:g.57017300A>T | GRCh37 |
| NC_000016.8:g.55574801A>T | NCBI36 |
| NG_008952.1:g.26466A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000200676.8:c.1384A>T MANE Select | ENSP00000200676.3:p.Asn462Tyr | |
| ENST00000650358.1:n.1782A>T | ||
| ENST00000200676.7:c.1384A>T | ENSP00000200676.3:p.Asn462Tyr | |
| ENST00000379780.6:c.1204A>T | ENSP00000369106.2:p.Asn402Tyr | |
| ENST00000566128.1:c.1189A>T | ENSP00000456276.1:p.Asn397Tyr | |
| NM_000078.2:c.1384A>T | NP_000069.2:p.Asn462Tyr | |
| NM_001286085.1:c.1204A>T | NP_001273014.1:p.Asn402Tyr | |
| NM_000078.3:c.1384A>T MANE Select | NP_000069.2:p.Asn462Tyr | |
| NM_001286085.2:c.1204A>T | NP_001273014.1:p.Asn402Tyr |