HGVS | Genome Assembly |
---|---|
NC_000008.11:g.98157729T>A , CM000670.2:g.98157729T>A | GRCh38 |
NC_000008.10:g.99169957T>A , CM000670.1:g.99169957T>A | GRCh37 |
NC_000008.9:g.99239133T>A | NCBI36 |
NG_052869.1:g.45437T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000401707.7:c.2533T>A MANE Select | ENSP00000385787.2:p.Cys845Ser | |
ENST00000349693.3:c.2533T>A | ENSP00000339529.3:p.Cys845Ser | |
ENST00000401707.6:c.2533T>A | ENSP00000385787.2:p.Cys845Ser | |
NM_001145860.1:c.2533T>A | NP_001139332.1:p.Cys845Ser | |
NM_001145861.1:c.2533T>A | NP_001139333.1:p.Cys845Ser | |
NM_015029.2:c.2533T>A | NP_055844.2:p.Cys845Ser | |
NM_001145860.2:c.2533T>A MANE Select | NP_001139332.1:p.Cys845Ser | |
NM_001145861.2:c.2533T>A | NP_001139333.1:p.Cys845Ser | |
NM_015029.3:c.2533T>A | NP_055844.2:p.Cys845Ser |