HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74919821C= , CM000679.2:g.74919821C= | GRCh38 |
NC_000017.10:g.72915916C= , CM000679.1:g.72915916C= | GRCh37 |
NC_000017.9:g.70427511C= | NCBI36 |
NG_007882.1:g.8436G= | |
NG_033062.1:g.547C= | |
NG_007882.2:g.8443G= | |
NG_033062.2:g.547C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614341.5:c.1015G= MANE Select | ENSP00000480279.1:p.Val339= | |
ENST00000579243.1:c.*614G= | ENSP00000462568.1:n.*614G= | |
ENST00000614341.4:c.1015G= | ENSP00000480279.1:p.Val339= | |
NM_001282489.2:c.706G= | NP_001269418.1:p.Val236= | |
NM_173477.4:c.1015G= | NP_775748.2:p.Val339= | |
XM_011524296.1:c.706G= | XP_011522598.1:p.Val236= | |
XM_011524296.2:c.706G= | XP_011522598.1:p.Val236= | |
NM_173477.5:c.1015G= MANE Select | NP_775748.2:p.Val339= | |
NM_001282489.3:c.706G= | NP_001269418.1:p.Val236= |