HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38408942A>C , CM000685.2:g.38408942A>C | GRCh38 |
NC_000023.10:g.38268195A>C , CM000685.1:g.38268195A>C | GRCh37 |
NC_000023.9:g.38153139A>C | NCBI36 |
NG_008471.1:g.61460A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000039007.5:c.784A>C MANE Select | ENSP00000039007.4:p.Thr262Pro | |
ENST00000643344.1:c.*534A>C | ENSP00000496606.1:n.*534A>C | |
ENST00000039007.4:c.784A>C | ENSP00000039007.4:p.Thr262Pro | |
ENST00000465127.1:c.172-257179A>C | ENSP00000417050.1:n.172-257179A>C | |
NM_000531.5:c.784A>C | NP_000522.3:p.Thr262Pro | |
XM_017029556.1:c.784A>C | XP_016885045.1:p.Thr262Pro | |
NM_000531.6:c.784A>C MANE Select | NP_000522.3:p.Thr262Pro |