Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714199C>G , CM000681.2:g.6714199C>G | GRCh38 |
| NC_000019.9:g.6714210C>G , CM000681.1:g.6714210C>G | GRCh37 |
| NC_000019.8:g.6665210C>G | NCBI36 |
| NG_009557.1:g.11453G>C , LRG_27:g.11453G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.526G>C | ENSP00000512083.1:p.Val176Leu | |
| ENST00000245907.11:c.649G>C MANE Select | ENSP00000245907.4:p.Val217Leu | |
| ENST00000245907.10:c.649G>C | ENSP00000245907.4:p.Val217Leu | |
| ENST00000595577.1:n.153G>C | ||
| NM_000064.3:c.649G>C | NP_000055.2:p.Val217Leu | |
| NM_000064.4:c.649G>C MANE Select | NP_000055.2:p.Val217Leu |