HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186197593C= , CM000666.2:g.186197593C= | GRCh38 |
NC_000004.11:g.187118747C= , CM000666.1:g.187118747C= | GRCh37 |
NC_000004.10:g.187355741C= | NCBI36 |
NG_007965.1:g.11074C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378802.5:c.665C= MANE Select | ENSP00000368079.4:p.Ala222= | |
ENST00000378802.4:c.665C= | ENSP00000368079.4:p.Ala222= | |
ENST00000507209.5:n.1506C= | ||
NM_207352.3:c.665C= | NP_997235.3:p.Ala222= | |
XM_005262935.2:c.665C= | XP_005262992.1:p.Ala222= | |
XM_006714184.2:c.269C= | XP_006714247.1:p.Ala90= | |
XM_005262935.4:c.665C= | XP_005262992.1:p.Ala222= | |
XM_017008037.1:c.269C= | XP_016863526.1:p.Ala90= | |
NM_207352.4:c.665C= MANE Select | NP_997235.3:p.Ala222= |