HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48342686A= , CM000675.2:g.48342686A= | GRCh38 |
NC_000013.10:g.48916822A= , CM000675.1:g.48916822A= | GRCh37 |
NC_000013.9:g.47814823A= | NCBI36 |
NG_009009.1:g.43940A= , LRG_517:g.43940A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.352A= MANE Select | ENSP00000267163.4:p.Thr118= | |
ENST00000650461.1:c.352A= | ENSP00000497193.1:p.Thr118= | |
ENST00000267163.4:c.352A= | ENSP00000267163.4:p.Thr118= | |
ENST00000467505.5:c.138-17331A= | ENSP00000434702.1:n.138-17331A= | |
ENST00000525036.1:n.514A= | ||
NM_000321.2:c.352A= , LRG_517t1:c.352A= | NP_000312.2:p.Thr118= | |
XM_011535171.1:c.91A= | XP_011533473.1:p.Thr31= | |
XM_011535171.2:c.91A= | XP_011533473.1:p.Thr31= | |
NM_000321.3:c.352A= MANE Select | NP_000312.2:p.Thr118= |