HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48468481T>C , CM000677.2:g.48468481T>C | GRCh38 |
NC_000015.9:g.48760678T>C , CM000677.1:g.48760678T>C | GRCh37 |
NC_000015.8:g.46547970T>C | NCBI36 |
NG_008805.2:g.182308A>G , LRG_778:g.182308A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.4513A>G | ENSP00000453958.2:p.Thr1505Ala | |
ENST00000674301.2:c.4513A>G | ENSP00000501333.2:p.Thr1505Ala | |
ENST00000684448.1:n.3187A>G | ||
ENST00000316623.10:c.4513A>G MANE Select | ENSP00000325527.5:p.Thr1505Ala | |
ENST00000316623.9:c.4513A>G | ENSP00000325527.5:p.Thr1505Ala | |
ENST00000537463.6:c.*276A>G | ENSP00000440294.2:n.*276A>G | |
NM_000138.4:c.4513A>G , LRG_778t1:c.4513A>G | NP_000129.3:p.Thr1505Ala | |
NM_000138.5:c.4513A>G MANE Select | NP_000129.3:p.Thr1505Ala |