HGVS | Genome Assembly |
---|---|
NC_000017.11:g.43755720G= , CM000679.2:g.43755720G= | GRCh38 |
NC_000017.10:g.41833088G= , CM000679.1:g.41833088G= | GRCh37 |
NC_000017.9:g.39188614G= | NCBI36 |
NG_008078.2:g.8069C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301691.3:c.264C= MANE Select | ENSP00000301691.1:p.Tyr88= | |
ENST00000301691.2:c.264C= | ENSP00000301691.1:p.Tyr88= | |
NM_025237.2:c.264C= | NP_079513.1:p.Tyr88= | |
NM_025237.3:c.264C= MANE Select | NP_079513.1:p.Tyr88= |