Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2445397T>G , CM000673.2:g.2445397T>G | GRCh38 |
| NC_000011.9:g.2466627T>G , CM000673.1:g.2466627T>G | GRCh37 |
| NC_000011.8:g.2423203T>G | NCBI36 |
| NG_008935.1:g.5407T>G , LRG_287:g.5407T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.38T>G | ENSP00000434560.2:p.Val13Gly | |
| ENST00000646564.2:c.299T>G | ENSP00000495806.2:p.Val100Gly | |
| ENST00000155840.12:c.299T>G MANE Select | ENSP00000155840.2:p.Val100Gly | |
| ENST00000155840.9:c.299T>G | ENSP00000155840.2:p.Val100Gly | |
| ENST00000345015.4:n.76T>G | ||
| ENST00000496887.6:c.38T>G | ENSP00000434560.1:p.Val13Gly | |
| NM_000218.2:c.299T>G , LRG_287t1:c.299T>G | NP_000209.2:p.Val100Gly | |
| NM_000218.3:c.299T>G MANE Select | NP_000209.2:p.Val100Gly |