HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86576009T>G , CM000670.2:g.86576009T>G | GRCh38 |
NC_000008.10:g.87588237T>G , CM000670.1:g.87588237T>G | GRCh37 |
NC_000008.9:g.87657353T>G | NCBI36 |
NG_016980.1:g.172667A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.2225A>C MANE Select | ENSP00000316605.5:p.Lys742Thr | |
ENST00000681546.1:n.2045A>C | ||
ENST00000681746.1:c.*636A>C | ENSP00000505959.1:n.*636A>C | |
ENST00000320005.5:c.2225A>C | ENSP00000316605.5:p.Lys742Thr | |
ENST00000517327.5:c.276+2680A>C | ENSP00000428329.1:n.276+2680A>C | |
NM_019098.4:c.2225A>C | NP_061971.3:p.Lys742Thr | |
XM_011517138.1:c.1811A>C | XP_011515440.1:p.Lys604Thr | |
XM_011517138.2:c.1811A>C | XP_011515440.1:p.Lys604Thr | |
NM_019098.5:c.2225A>C MANE Select | NP_061971.3:p.Lys742Thr |