HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186197592G= , CM000666.2:g.186197592G= | GRCh38 |
NC_000004.11:g.187118746G= , CM000666.1:g.187118746G= | GRCh37 |
NC_000004.10:g.187355740G= | NCBI36 |
NG_007965.1:g.11073G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378802.5:c.664G= MANE Select | ENSP00000368079.4:p.Ala222= | |
ENST00000378802.4:c.664G= | ENSP00000368079.4:p.Ala222= | |
ENST00000507209.5:n.1505G= | ||
NM_207352.3:c.664G= | NP_997235.3:p.Ala222= | |
XM_005262935.2:c.664G= | XP_005262992.1:p.Ala222= | |
XM_006714184.2:c.268G= | XP_006714247.1:p.Ala90= | |
XM_005262935.4:c.664G= | XP_005262992.1:p.Ala222= | |
XM_017008037.1:c.268G= | XP_016863526.1:p.Ala90= | |
NM_207352.4:c.664G= MANE Select | NP_997235.3:p.Ala222= |