HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74919623C>T , CM000679.2:g.74919623C>T | GRCh38 |
NC_000017.10:g.72915718C>T , CM000679.1:g.72915718C>T | GRCh37 |
NC_000017.9:g.70427313C>T | NCBI36 |
NG_007882.1:g.8634G>A | |
NG_033062.1:g.349C>T | |
NG_007882.2:g.8641G>A | |
NG_033062.2:g.349C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614341.5:c.1213G>A MANE Select | ENSP00000480279.1:p.Ala405Thr | |
ENST00000579243.1:c.*812G>A | ENSP00000462568.1:n.*812G>A | |
ENST00000614341.4:c.1213G>A | ENSP00000480279.1:p.Ala405Thr | |
NM_001282489.2:c.904G>A | NP_001269418.1:p.Ala302Thr | |
NM_173477.4:c.1213G>A | NP_775748.2:p.Ala405Thr | |
XM_011524296.1:c.904G>A | XP_011522598.1:p.Ala302Thr | |
XM_011524296.2:c.904G>A | XP_011522598.1:p.Ala302Thr | |
NM_173477.5:c.1213G>A MANE Select | NP_775748.2:p.Ala405Thr | |
NM_001282489.3:c.904G>A | NP_001269418.1:p.Ala302Thr |