HGVS | Genome Assembly |
---|---|
NC_000005.10:g.136056785C= , CM000667.2:g.136056785C= | GRCh38 |
NC_000005.9:g.135392474C= , CM000667.1:g.135392474C= | GRCh37 |
NC_000005.8:g.135420373C= | NCBI36 |
NG_012646.1:g.32891C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000442011.7:c.1668C= MANE Select | ENSP00000416330.2:p.Ser556= | |
ENST00000442011.6:c.1668C= | ENSP00000416330.2:p.Ser556= | |
ENST00000506699.5:n.2185C= | ||
ENST00000507018.5:c.1646C= | ||
ENST00000509485.5:c.665C= | ||
ENST00000514242.5:n.439C= | ||
ENST00000514554.5:c.820C= | ||
NM_000358.2:c.1668C= | NP_000349.1:p.Ser556= | |
NM_000358.3:c.1668C= MANE Select | NP_000349.1:p.Ser556= |