HGVS | Genome Assembly |
---|---|
NC_000016.10:g.1985892G= , CM000678.2:g.1985892G= | GRCh38 |
NC_000016.9:g.2035893G= , CM000678.1:g.2035893G= | GRCh37 |
NC_000016.8:g.1975894G= | NCBI36 |
NG_016288.1:g.6744G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000567719.2:c.257G= | ENSP00000455885.1:p.Arg86= | |
ENST00000248114.7:c.482G= MANE Select | ENSP00000248114.6:p.Arg161= | |
ENST00000248114.6:c.482G= | ENSP00000248114.6:p.Arg161= | |
ENST00000565658.1:n.639G= | ||
ENST00000567719.1:c.257G= | ENSP00000455885.1:p.Arg86= | |
ENST00000569451.1:c.285G= | ENSP00000456432.1:p.Pro95= | |
NM_005262.2:c.482G= | NP_005253.3:p.Arg161= | |
NM_005262.3:c.482G= MANE Select | NP_005253.3:p.Arg161= |