HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48476807G= , CM000675.2:g.48476807G= | GRCh38 |
NC_000013.10:g.49050943G= , CM000675.1:g.49050943G= | GRCh37 |
NC_000013.9:g.47948944G= | NCBI36 |
NG_009009.1:g.178061G= , LRG_517:g.178061G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.2627G= MANE Select | ENSP00000267163.4:p.Arg876= | |
ENST00000643064.1:c.194+95364G= | ||
ENST00000650461.1:c.2627G= | ENSP00000497193.1:p.Arg876= | |
ENST00000267163.4:c.2627G= | ENSP00000267163.4:p.Arg876= | |
ENST00000484879.1:n.361G= | ||
ENST00000531171.5:n.230G= | ||
NM_000321.2:c.2627G= , LRG_517t1:c.2627G= | NP_000312.2:p.Arg876= | |
XM_011535171.1:c.2366G= | XP_011533473.1:p.Arg789= | |
XM_011535171.2:c.2366G= | XP_011533473.1:p.Arg789= | |
NM_000321.3:c.2627G= MANE Select | NP_000312.2:p.Arg876= |