HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17018942T>G , CM000663.2:g.17018942T>G | GRCh38 |
NC_000001.10:g.17345437T>G , CM000663.1:g.17345437T>G | GRCh37 |
NC_000001.9:g.17218024T>G | NCBI36 |
NG_012340.1:g.40229A>C , LRG_316:g.40229A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.611A>C | ENSP00000481376.2:p.Lys204Thr | |
ENST00000491274.6:c.740A>C | ENSP00000480482.2:p.Lys247Thr | |
ENST00000375499.8:c.782A>C MANE Select | ENSP00000364649.3:p.Lys261Thr | |
ENST00000375499.7:c.782A>C | ENSP00000364649.3:p.Lys261Thr | |
ENST00000475049.5:n.207A>C | ||
ENST00000485092.5:n.446A>C | ||
NM_003000.2:c.782A>C , LRG_316t1:c.782A>C | NP_002991.2:p.Lys261Thr | |
NM_003000.3:c.782A>C MANE Select | NP_002991.2:p.Lys261Thr |