HGVS | Genome Assembly |
---|---|
NC_000023.11:g.47572877A>C , CM000685.2:g.47572877A>C | GRCh38 |
NC_000023.10:g.47432276A>C , CM000685.1:g.47432276A>C | GRCh37 |
NC_000023.9:g.47317220A>C | NCBI36 |
NG_008437.1:g.51981T>G | |
NG_016339.1:g.16761A>C | |
NG_016339.2:g.16761A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295987.13:c.2105T>G MANE Select | ENSP00000295987.7:p.Leu702Arg | |
ENST00000340666.5:c.*57T>G | ENSP00000343206.4:n.*57T>G | |
ENST00000640721.1:c.155T>G | ENSP00000492857.1:p.Leu52Arg | |
ENST00000295987.11:c.2105T>G | ENSP00000295987.7:p.Leu702Arg | |
ENST00000340666.4:c.*57T>G | ENSP00000343206.4:n.*57T>G | |
NM_006950.3:c.2105T>G MANE Select | NP_008881.2:p.Leu702Arg | |
NM_133499.2:c.*57T>G | NP_598006.1:n.*57T>G |