HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18783031C= , CM000681.2:g.18783031C= | GRCh38 |
NC_000019.9:g.18893841C= , CM000681.1:g.18893841C= | GRCh37 |
NC_000019.8:g.18754841C= | NCBI36 |
NG_007070.1:g.13274G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000222271.7:c.2227+23G= MANE Select | ENSP00000222271.2:n.2227+23G= | |
ENST00000222271.6:c.2227+23G= | ENSP00000222271.2:n.2227+23G= | |
ENST00000425807.1:c.2068+23G= | ENSP00000403792.1:n.2068+23G= | |
ENST00000542601.6:c.2128+23G= | ENSP00000439156.2:n.2128+23G= | |
NM_000095.2:c.2227+23G= | NP_000086.2:n.2227+23G= | |
NM_000095.3:c.2227+23G= MANE Select | NP_000086.2:n.2227+23G= |