HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47333750G>A , CM000673.2:g.47333750G>A | GRCh38 |
NC_000011.9:g.47355301G>A , CM000673.1:g.47355301G>A | GRCh37 |
NC_000011.8:g.47311877G>A | NCBI36 |
NG_007667.1:g.23953C>T , LRG_386:g.23953C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000545968.6:c.2997C>T MANE Select | ENSP00000442795.1:p.Gly999= | |
ENST00000256993.8:c.2997C>T | ENSP00000256993.5:p.Gly999= | |
ENST00000399249.6:c.2997C>T | ENSP00000382193.2:p.Gly999= | |
ENST00000545968.5:c.2997C>T | ENSP00000442795.1:p.Gly999= | |
NM_000256.3:c.2997C>T , LRG_386t1:c.2997C>T MANE Select | NP_000247.2:p.Gly999= | |
XM_011520117.1:c.2979C>T | XP_011518419.1:p.Gly993= | |
XM_011520118.1:c.2916C>T | XP_011518420.1:p.Gly972= |