HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65239929G>T , CM000674.2:g.65239929G>T | GRCh38 |
NC_000012.11:g.65633709G>T , CM000674.1:g.65633709G>T | GRCh37 |
NC_000012.10:g.63919976G>T | NCBI36 |
NG_016210.1:g.75359G>T | |
NG_016210.2:g.75359G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.1922G>T MANE Select | ENSP00000308369.2:p.Gly641Val | |
ENST00000308330.2:c.1922G>T | ENSP00000308369.2:p.Gly641Val | |
NM_001167614.1:c.1919G>T | NP_001161086.1:p.Gly640Val | |
NM_014319.4:c.1922G>T | NP_055134.2:p.Gly641Val | |
NM_014319.5:c.1922G>T MANE Select | NP_055134.2:p.Gly641Val | |
NM_001167614.2:c.1919G>T | NP_001161086.1:p.Gly640Val |