HGVS | Genome Assembly |
---|---|
NC_000023.11:g.47574527G>C , CM000685.2:g.47574527G>C | GRCh38 |
NC_000023.10:g.47433926G>C , CM000685.1:g.47433926G>C | GRCh37 |
NC_000023.9:g.47318870G>C | NCBI36 |
NG_008437.1:g.50331C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295987.13:c.1457C>G MANE Select | ENSP00000295987.7:p.Pro486Arg | |
ENST00000340666.5:c.1457C>G | ENSP00000343206.4:p.Pro486Arg | |
ENST00000640721.1:c.70+161C>G | ENSP00000492857.1:n.70+161C>G | |
ENST00000295987.11:c.1457C>G | ENSP00000295987.7:p.Pro486Arg | |
ENST00000340666.4:c.1457C>G | ENSP00000343206.4:p.Pro486Arg | |
NM_006950.3:c.1457C>G MANE Select | NP_008881.2:p.Pro486Arg | |
NM_133499.2:c.1457C>G | NP_598006.1:p.Pro486Arg |