Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110601655A>G , CM000672.2:g.110601655A>G | GRCh38 |
| NC_000010.10:g.112361413A>G , CM000672.1:g.112361413A>G | GRCh37 |
| NC_000010.9:g.112351403A>G | NCBI36 |
| NG_012217.1:g.38965A>G , LRG_774:g.38965A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.4896A>G | ||
| ENST00000685743.1:n.2371A>G | ||
| ENST00000686057.1:n.1014A>G | ||
| ENST00000689321.1:n.1626A>G | ||
| ENST00000689986.1:n.452A>G | ||
| ENST00000361804.5:c.2663A>G MANE Select | ENSP00000354720.5:p.Asp888Gly | |
| ENST00000361804.4:c.2663A>G | ENSP00000354720.4:p.Asp888Gly | |
| NM_005445.3:c.2663A>G , LRG_774t1:c.2663A>G | NP_005436.1:p.Asp888Gly | |
| NM_005445.4:c.2663A>G MANE Select | NP_005436.1:p.Asp888Gly |