HGVS | Genome Assembly |
---|---|
NC_000014.9:g.50909979A>G , CM000676.2:g.50909979A>G | GRCh38 |
NC_000014.8:g.51376697A>G , CM000676.1:g.51376697A>G | GRCh37 |
NC_000014.7:g.50446447A>G | NCBI36 |
NG_012796.1:g.39552T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216392.8:c.2093T>C MANE Select | ENSP00000216392.7:p.Val698Ala | |
ENST00000216392.7:c.2093T>C | ENSP00000216392.7:p.Val698Ala | |
ENST00000532107.2:n.266T>C | ||
ENST00000532462.5:c.2093T>C | ENSP00000431657.1:p.Val698Ala | |
ENST00000544180.6:c.1991T>C | ENSP00000443787.1:p.Val664Ala | |
NM_001163940.1:c.1991T>C | NP_001157412.1:p.Val664Ala | |
NM_002863.4:c.2093T>C | NP_002854.3:p.Val698Ala | |
NM_002863.5:c.2093T>C MANE Select | NP_002854.3:p.Val698Ala | |
NM_001163940.2:c.1991T>C | NP_001157412.1:p.Val664Ala |