HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86576097C>G , CM000670.2:g.86576097C>G | GRCh38 |
NC_000008.10:g.87588325C>G , CM000670.1:g.87588325C>G | GRCh37 |
NC_000008.9:g.87657441C>G | NCBI36 |
NG_016980.1:g.172579G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.2137G>C MANE Select | ENSP00000316605.5:p.Gly713Arg | |
ENST00000681546.1:n.1957G>C | ||
ENST00000681746.1:c.*548G>C | ENSP00000505959.1:n.*548G>C | |
ENST00000320005.5:c.2137G>C | ENSP00000316605.5:p.Gly713Arg | |
ENST00000517327.5:c.276+2592G>C | ENSP00000428329.1:n.276+2592G>C | |
NM_019098.4:c.2137G>C | NP_061971.3:p.Gly713Arg | |
XM_011517138.1:c.1723G>C | XP_011515440.1:p.Gly575Arg | |
XM_011517138.2:c.1723G>C | XP_011515440.1:p.Gly575Arg | |
NM_019098.5:c.2137G>C MANE Select | NP_061971.3:p.Gly713Arg |