HGVS | Genome Assembly |
---|---|
NC_000006.12:g.6224809A>C , CM000668.2:g.6224809A>C | GRCh38 |
NC_000006.11:g.6225042A>C , CM000668.1:g.6225042A>C | GRCh37 |
NC_000006.10:g.6170041A>C | NCBI36 |
NG_008107.1:g.100883T>G , LRG_549:g.100883T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264870.8:c.850T>G MANE Select | ENSP00000264870.3:p.Tyr284Asp | |
ENST00000264870.7:c.850T>G | ENSP00000264870.3:p.Tyr284Asp | |
NM_000129.3:c.850T>G , LRG_549t1:c.850T>G | NP_000120.2:p.Tyr284Asp | |
XM_006715010.2:c.850T>G | XP_006715073.1:p.Tyr284Asp | |
XM_011514342.1:c.1012T>G | XP_011512644.1:p.Tyr338Asp | |
NM_000129.4:c.850T>G MANE Select | NP_000120.2:p.Tyr284Asp |