Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.146340214A>T , CM000667.2:g.146340214A>T | GRCh38 |
| NC_000005.9:g.145719777A>T , CM000667.1:g.145719777A>T | GRCh37 |
| NC_000005.8:g.145699970A>T | NCBI36 |
| NG_011885.1:g.6191A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000646991.2:c.787A>T MANE Select | ENSP00000495718.1:p.Asn263Tyr | |
| ENST00000230732.4:c.787A>T | ENSP00000230732.4:p.Asn263Tyr | |
| NM_002700.2:c.787A>T | NP_002691.1:p.Asn263Tyr | |
| NM_002700.3:c.787A>T MANE Select | NP_002691.1:p.Asn263Tyr |