HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114679624C= , CM000663.2:g.114679624C= | GRCh38 |
NC_000001.10:g.115222245C= , CM000663.1:g.115222245C= | GRCh37 |
NC_000001.9:g.115023768C= | NCBI36 |
NG_008012.1:g.20932G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369538.4:c.840G= | ENSP00000358551.4:p.Lys280= | |
ENST00000520113.7:c.852G= MANE Select | ENSP00000430075.3:p.Lys284= | |
ENST00000637080.1:c.635G= | ENSP00000489753.1:n.635G= | |
ENST00000639077.1:n.517G= | ||
ENST00000369538.3:c.939G= | ENSP00000358551.3:p.Lys313= | |
ENST00000520113.6:c.951G= | ENSP00000430075.2:p.Lys317= | |
NM_000036.2:c.951G= | NP_000027.2:p.Lys317= | |
NM_001172626.1:c.939G= | NP_001166097.1:p.Lys313= | |
NM_000036.3:c.852G= MANE Select | NP_000027.3:p.Lys284= | |
NM_001172626.2:c.840G= | NP_001166097.2:p.Lys280= |