HGVS | Genome Assembly |
---|---|
NC_000023.11:g.50192917T>C , CM000685.2:g.50192917T>C | GRCh38 |
NC_000023.10:g.49957568T>C , CM000685.1:g.49957568T>C | GRCh37 |
NC_000023.9:g.49844308T>C | NCBI36 |
NG_012552.1:g.13097A>G | |
NG_012552.2:g.13097A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000358526.7:c.1796A>G MANE Select | ENSP00000351327.2:p.Lys599Arg | |
ENST00000358526.6:c.1796A>G | ENSP00000351327.2:p.Lys599Arg | |
ENST00000376064.7:c.1769A>G | ENSP00000365232.3:p.Lys590Arg | |
ENST00000481402.5:n.1908A>G | ||
NM_003886.2:c.1796A>G | NP_003877.2:p.Lys599Arg | |
NM_139289.1:c.1769A>G | NP_647450.1:p.Lys590Arg | |
NM_003886.3:c.1796A>G MANE Select | NP_003877.2:p.Lys599Arg | |
NM_139289.2:c.1769A>G | NP_647450.1:p.Lys590Arg |