HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320402C= , CM000667.2:g.159320402C= | GRCh38 |
NC_000005.9:g.158747410C= , CM000667.1:g.158747410C= | GRCh37 |
NC_000005.8:g.158679988C= | NCBI36 |
NG_009618.1:g.15072G= , LRG_71:g.15072G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.-30G= | ENSP00000512849.1:n.-30G= | |
ENST00000696751.1:c.*96G= | ENSP00000512850.1:n.*96G= | |
ENST00000231228.3:c.601G= MANE Select | ENSP00000231228.2:p.Ala201= | |
ENST00000231228.2:c.601G= | ENSP00000231228.2:p.Ala201= | |
NM_002187.2:c.601G= , LRG_71t1:c.601G= | NP_002178.2:p.Ala201= | |
NM_002187.3:c.601G= MANE Select | NP_002178.2:p.Ala201= |