HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48476744G= , CM000675.2:g.48476744G= | GRCh38 |
NC_000013.10:g.49050880G= , CM000675.1:g.49050880G= | GRCh37 |
NC_000013.9:g.47948881G= | NCBI36 |
NG_009009.1:g.177998G= , LRG_517:g.177998G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.2564G= MANE Select | ENSP00000267163.4:p.Ser855= | |
ENST00000643064.1:c.194+95301G= | ||
ENST00000650461.1:c.2564G= | ENSP00000497193.1:p.Ser855= | |
ENST00000267163.4:c.2564G= | ENSP00000267163.4:p.Ser855= | |
ENST00000484879.1:n.298G= | ||
ENST00000531171.5:n.167G= | ||
NM_000321.2:c.2564G= , LRG_517t1:c.2564G= | NP_000312.2:p.Ser855= | |
XM_011535171.1:c.2303G= | XP_011533473.1:p.Ser768= | |
XM_011535171.2:c.2303G= | XP_011533473.1:p.Ser768= | |
NM_000321.3:c.2564G= MANE Select | NP_000312.2:p.Ser855= |