Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.149569991T>A , CM000664.2:g.149569991T>A | GRCh38 |
| NC_000002.11:g.150426505T>A , CM000664.1:g.150426505T>A | GRCh37 |
| NC_000002.10:g.150134751T>A | NCBI36 |
| NG_009189.1:g.22826A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000303319.10:c.874A>T MANE Select | ENSP00000301920.5:p.Lys292Ter | |
| ENST00000303319.9:c.874A>T | ENSP00000301920.5:p.Lys292Ter | |
| ENST00000422782.2:c.976A>T | ENSP00000408331.2:p.Lys326Ter | |
| ENST00000428879.5:c.874A>T | ENSP00000389060.1:p.Lys292Ter | |
| NM_015702.2:c.874A>T | NP_056517.1:p.Lys292Ter | |
| NM_015702.3:c.874A>T MANE Select | NP_056517.1:p.Lys292Ter |