HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86575980C= , CM000670.2:g.86575980C= | GRCh38 |
NC_000008.10:g.87588208C= , CM000670.1:g.87588208C= | GRCh37 |
NC_000008.9:g.87657324C= | NCBI36 |
NG_016980.1:g.172696G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000320005.6:c.2254G= MANE Select | ENSP00000316605.5:p.Asp752= | |
ENST00000681546.1:n.2074G= | ||
ENST00000681746.1:c.*665G= | ENSP00000505959.1:n.*665G= | |
ENST00000320005.5:c.2254G= | ENSP00000316605.5:p.Asp752= | |
ENST00000517327.5:c.276+2709G= | ENSP00000428329.1:n.276+2709G= | |
NM_019098.4:c.2254G= | NP_061971.3:p.Asp752= | |
XM_011517138.1:c.1840G= | XP_011515440.1:p.Asp614= | |
XM_011517138.2:c.1840G= | XP_011515440.1:p.Asp614= | |
NM_019098.5:c.2254G= MANE Select | NP_061971.3:p.Asp752= |