HGVS | Genome Assembly |
---|---|
NC_000012.12:g.89350762A>T , CM000674.2:g.89350762A>T | GRCh38 |
NC_000012.11:g.89744539A>T , CM000674.1:g.89744539A>T | GRCh37 |
NC_000012.10:g.88268670A>T | NCBI36 |
NG_033915.1:g.7098T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000279488.8:c.664T>A MANE Select | ENSP00000279488.6:p.Ser222Thr | |
ENST00000279488.7:c.664T>A | ENSP00000279488.6:p.Ser222Thr | |
ENST00000308385.6:c.400+878T>A | ENSP00000307835.6:n.400+878T>A | |
ENST00000547140.1:n.350T>A | ||
ENST00000547291.1:c.289T>A | ENSP00000449838.1:p.Ser97Thr | |
NM_001946.3:c.664T>A | NP_001937.2:p.Ser222Thr | |
NM_022652.3:c.400+878T>A | NP_073143.2:n.400+878T>A | |
NM_001946.4:c.664T>A MANE Select | NP_001937.2:p.Ser222Thr | |
NM_022652.4:c.400+878T>A | NP_073143.2:n.400+878T>A |