HGVS | Genome Assembly |
---|---|
NC_000014.9:g.28768672A>G , CM000676.2:g.28768672A>G | GRCh38 |
NC_000014.8:g.29237878A>G , CM000676.1:g.29237878A>G | GRCh37 |
NC_000014.7:g.28307629A>G | NCBI36 |
NG_009367.1:g.6592A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706482.1:c.1393A>G | ENSP00000516406.1:p.Thr465Ala | |
ENST00000313071.7:c.1393A>G MANE Select | ENSP00000339004.3:p.Thr465Ala | |
ENST00000313071.6:c.1393A>G | ENSP00000339004.3:p.Thr465Ala | |
NM_005249.4:c.1393A>G | NP_005240.3:p.Thr465Ala | |
NM_005249.5:c.1393A>G MANE Select | NP_005240.3:p.Thr465Ala |