HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55043984G= , CM000663.2:g.55043984G= | GRCh38 |
NC_000001.10:g.55509657G= , CM000663.1:g.55509657G= | GRCh37 |
NC_000001.9:g.55282245G= | NCBI36 |
NG_009061.1:g.9438G= , LRG_275:g.9438G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.349G= | ENSP00000501161.2:p.Gly117= | |
ENST00000710286.1:c.706G= | ENSP00000518176.1:p.Gly236= | |
ENST00000673662.1:n.19G= | ||
ENST00000673726.1:c.349G= | ENSP00000501004.1:p.Gly117= | |
ENST00000673903.1:c.-27G= | ENSP00000501257.1:n.-27G= | |
ENST00000302118.5:c.349G= MANE Select | ENSP00000303208.5:p.Gly117= | |
NM_174936.3:c.349G= , LRG_275t1:c.349G= | NP_777596.2:p.Gly117= | |
NR_110451.1:n.182+3581G= | ||
NM_174936.4:c.349G= MANE Select | NP_777596.2:p.Gly117= | |
NR_110451.2:n.182+3581G= |