Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659096A>G , CM000685.2:g.136659096A>G | GRCh38 |
| NC_000023.10:g.135741255A>G , CM000685.1:g.135741255A>G | GRCh37 |
| NC_000023.9:g.135568921A>G | NCBI36 |
| NG_007280.1:g.15920A>G , LRG_141:g.15920A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000695724.1:c.*85A>G | ENSP00000512122.1:n.*85A>G | |
| ENST00000695725.1:c.*22A>G | ENSP00000512123.1:n.*22A>G | |
| ENST00000695726.1:n.2435A>G | ||
| ENST00000695729.1:n.3270A>G | ||
| ENST00000370629.7:c.467A>G MANE Select | ENSP00000359663.2:p.Glu156Gly | |
| ENST00000370628.2:c.404A>G | ENSP00000359662.2:p.Glu135Gly | |
| ENST00000370629.6:c.467A>G | ENSP00000359663.2:p.Glu156Gly | |
| NM_000074.2:c.467A>G , LRG_141t1:c.467A>G | NP_000065.1:p.Glu156Gly | |
| NM_000074.3:c.467A>G MANE Select | NP_000065.1:p.Glu156Gly |