HGVS | Genome Assembly |
---|---|
NC_000006.12:g.167341603G>T , CM000668.2:g.167341603G>T | GRCh38 |
NC_000006.11:g.167755091G>T , CM000668.1:g.167755091G>T | GRCh37 |
NC_000006.10:g.167675081G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000239587.10:c.1703G>T MANE Select | ENSP00000239587.5:p.Gly568Val | |
ENST00000649884.1:c.1484G>T | ENSP00000497040.1:p.Gly495Val | |
ENST00000239587.9:c.1703G>T | ENSP00000239587.5:p.Gly568Val | |
ENST00000515138.1:c.1703G>T | ENSP00000424130.1:p.Gly568Val | |
NM_031949.4:c.1703G>T | NP_114155.4:p.Gly568Val | |
XM_006715572.2:c.1484G>T | XP_006715635.1:p.Gly495Val | |
XM_006715572.4:c.1484G>T | XP_006715635.1:p.Gly495Val | |
NM_031949.5:c.1703G>T MANE Select | NP_114155.4:p.Gly568Val |