HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169485683T>A , CM000663.2:g.169485683T>A | GRCh38 |
NC_000001.10:g.169454921T>A , CM000663.1:g.169454921T>A | GRCh37 |
NC_000001.9:g.167721545T>A | NCBI36 |
NG_008255.1:g.5288A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000236137.10:c.84A>T MANE Select | ENSP00000236137.5:p.Glu28Asp | |
ENST00000646596.1:c.84A>T | ENSP00000494404.1:p.Glu28Asp | |
ENST00000236137.9:c.84A>T | ENSP00000236137.5:p.Glu28Asp | |
ENST00000367804.4:c.84A>T | ENSP00000356778.3:p.Glu28Asp | |
NM_006996.2:c.84A>T | NP_008927.1:p.Glu28Asp | |
XM_011509076.1:c.12+370A>T | XP_011507378.1:n.12+370A>T | |
XM_011509077.1:c.84A>T | XP_011507379.1:p.Glu28Asp | |
NM_001319667.1:c.84A>T | NP_001306596.1:p.Glu28Asp | |
NM_006996.3:c.84A>T MANE Select | NP_008927.1:p.Glu28Asp |