HGVS | Genome Assembly |
---|---|
NC_000014.9:g.50910013C>A , CM000676.2:g.50910013C>A | GRCh38 |
NC_000014.8:g.51376731C>A , CM000676.1:g.51376731C>A | GRCh37 |
NC_000014.7:g.50446481C>A | NCBI36 |
NG_012796.1:g.39518G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216392.8:c.2059G>T MANE Select | ENSP00000216392.7:p.Ala687Ser | |
ENST00000216392.7:c.2059G>T | ENSP00000216392.7:p.Ala687Ser | |
ENST00000532107.2:n.232G>T | ||
ENST00000532462.5:c.2059G>T | ENSP00000431657.1:p.Ala687Ser | |
ENST00000544180.6:c.1957G>T | ENSP00000443787.1:p.Ala653Ser | |
NM_001163940.1:c.1957G>T | NP_001157412.1:p.Ala653Ser | |
NM_002863.4:c.2059G>T | NP_002854.3:p.Ala687Ser | |
NM_002863.5:c.2059G>T MANE Select | NP_002854.3:p.Ala687Ser | |
NM_001163940.2:c.1957G>T | NP_001157412.1:p.Ala653Ser |