HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55043984G>C , CM000663.2:g.55043984G>C | GRCh38 |
NC_000001.10:g.55509657G>C , CM000663.1:g.55509657G>C | GRCh37 |
NC_000001.9:g.55282245G>C | NCBI36 |
NG_009061.1:g.9438G>C , LRG_275:g.9438G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.349G>C | ENSP00000501161.2:p.Gly117Arg | |
ENST00000710286.1:c.706G>C | ENSP00000518176.1:p.Gly236Arg | |
ENST00000673662.1:n.19G>C | ||
ENST00000673726.1:c.349G>C | ENSP00000501004.1:p.Gly117Arg | |
ENST00000673903.1:c.-27G>C | ENSP00000501257.1:n.-27G>C | |
ENST00000302118.5:c.349G>C MANE Select | ENSP00000303208.5:p.Gly117Arg | |
NM_174936.3:c.349G>C , LRG_275t1:c.349G>C | NP_777596.2:p.Gly117Arg | |
NR_110451.1:n.182+3581G>C | ||
NM_174936.4:c.349G>C MANE Select | NP_777596.2:p.Gly117Arg | |
NR_110451.2:n.182+3581G>C |