HGVS | Genome Assembly |
---|---|
NC_000022.11:g.17085006A>T , CM000684.2:g.17085006A>T | GRCh38 |
NC_000022.10:g.17565896A>T , CM000684.1:g.17565896A>T | GRCh37 |
NC_000022.9:g.15945896A>T | NCBI36 |
NG_028257.1:g.5046A>T , LRG_355:g.5046A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000694948.1:n.13A>T | ||
ENST00000694949.1:n.10A>T | ||
ENST00000319363.11:c.-86A>T MANE Select | ENSP00000320936.6:n.-86A>T | |
ENST00000319363.10:c.-86A>T | ENSP00000320936.6:n.-86A>T | |
ENST00000477874.1:n.53A>T | ||
ENST00000612619.1:c.-86A>T | ENSP00000479970.1:n.-86A>T | |
NM_001289905.1:c.-86A>T | NP_001276834.1:n.-86A>T | |
NM_014339.6:c.-86A>T , LRG_355t1:c.-86A>T | NP_055154.3:n.-86A>T | |
NM_014339.7:c.-86A>T MANE Select | NP_055154.3:n.-86A>T | |
NM_001289905.2:c.-86A>T | NP_001276834.1:n.-86A>T |