HGVS | Genome Assembly |
---|---|
NC_000006.12:g.33669026T>G , CM000668.2:g.33669026T>G | GRCh38 |
NC_000006.11:g.33636803T>G , CM000668.1:g.33636803T>G | GRCh37 |
NC_000006.10:g.33744781T>G | NCBI36 |
NG_027729.1:g.52648T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000605930.3:c.2059T>G MANE Select | ENSP00000475177.1:p.Tyr687Asp | |
ENST00000374316.9:c.2059T>G | ENSP00000363435.4:p.Tyr687Asp | |
ENST00000605930.2:c.2059T>G | ENSP00000475177.1:p.Tyr687Asp | |
NM_002224.3:c.2059T>G | NP_002215.2:p.Tyr687Asp | |
XM_011514576.1:c.2128T>G | XP_011512878.1:p.Tyr710Asp | |
XM_011514577.1:c.1876T>G | XP_011512879.1:p.Tyr626Asp | |
XM_011514577.3:c.1876T>G | XP_011512879.1:p.Tyr626Asp | |
XM_017010832.1:c.2059T>G | XP_016866321.1:p.Tyr687Asp | |
NM_002224.4:c.2059T>G MANE Select | NP_002215.2:p.Tyr687Asp |