Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240877586A>T , CM000664.2:g.240877586A>T | GRCh38 |
| NC_000002.11:g.241817003A>T , CM000664.1:g.241817003A>T | GRCh37 |
| NC_000002.10:g.241465676A>T | NCBI36 |
| NG_008005.1:g.13842A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.896A>T MANE Select | ENSP00000302620.3:p.His299Leu | |
| ENST00000307503.3:c.896A>T | ENSP00000302620.3:p.His299Leu | |
| ENST00000470255.1:n.674A>T | ||
| NM_000030.2:c.896A>T | NP_000021.1:p.His299Leu | |
| NM_000030.3:c.896A>T MANE Select | NP_000021.1:p.His299Leu |