HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18400088G= , CM000670.2:g.18400088G= | GRCh38 |
NC_000008.10:g.18257598G= , CM000670.1:g.18257598G= | GRCh37 |
NC_000008.9:g.18301878G= | NCBI36 |
NG_012246.1:g.13844G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286479.4:c.85G= MANE Select | ENSP00000286479.3:p.Glu29= | |
ENST00000286479.3:c.85G= | ENSP00000286479.3:p.Glu29= | |
ENST00000520116.1:c.-57-249G= | ENSP00000428416.1:n.-57-249G= | |
NM_000015.2:c.85G= | NP_000006.2:p.Glu29= | |
XM_011544358.1:c.85G= | XP_011542660.1:p.Glu29= | |
XM_017012938.1:c.85G= | XP_016868427.1:p.Glu29= | |
NM_000015.3:c.85G= MANE Select | NP_000006.2:p.Glu29= |