HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320366C= , CM000667.2:g.159320366C= | GRCh38 |
NC_000005.9:g.158747374C= , CM000667.1:g.158747374C= | GRCh37 |
NC_000005.8:g.158679952C= | NCBI36 |
NG_009618.1:g.15108G= , LRG_71:g.15108G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000696750.1:c.7G= | ENSP00000512849.1:p.Asp3= | |
ENST00000696751.1:c.*132G= | ENSP00000512850.1:n.*132G= | |
ENST00000231228.3:c.637G= MANE Select | ENSP00000231228.2:p.Asp213= | |
ENST00000231228.2:c.637G= | ENSP00000231228.2:p.Asp213= | |
NM_002187.2:c.637G= , LRG_71t1:c.637G= | NP_002178.2:p.Asp213= | |
NM_002187.3:c.637G= MANE Select | NP_002178.2:p.Asp213= |