HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88007784G= , CM000666.2:g.88007784G= | GRCh38 |
NC_000004.11:g.88928936G= , CM000666.1:g.88928936G= | GRCh37 |
NC_000004.10:g.89147960G= | NCBI36 |
NG_008604.1:g.5117G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237596.7:c.51G= MANE Select | ENSP00000237596.2:p.Arg17= | |
ENST00000237596.6:c.51G= | ENSP00000237596.2:p.Arg17= | |
NM_000297.3:c.51G= | NP_000288.1:p.Arg17= | |
XM_011532028.1:c.51G= | XP_011530330.1:p.Arg17= | |
XR_244632.2:n.146G= | ||
NR_156488.1:n.138G= | ||
XM_011532028.2:c.51G= | XP_011530330.1:p.Arg17= | |
NM_000297.4:c.51G= MANE Select | NP_000288.1:p.Arg17= | |
NR_156488.2:n.150G= |