HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73367854_73367855insA , CM000677.2:g.73367854_73367855insA | GRCh38 |
NC_000015.9:g.73660195_73660196insA , CM000677.1:g.73660195_73660196insA | GRCh37 |
NC_000015.8:g.71447248_71447249insA | NCBI36 |
NG_009063.1:g.6410_6411insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.416_417insT MANE Select | ENSP00000261917.3:p.Gly140ArgfsTer? | |
ENST00000261917.3:c.416_417insT | ENSP00000261917.3:p.Gly140ArgfsTer? | |
NM_005477.2:c.416_417insT | NP_005468.1:p.Gly140ArgfsTer? | |
NM_005477.3:c.416_417insT MANE Select | NP_005468.1:p.Gly140ArgfsTer? |