HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48348965T>A , CM000675.2:g.48348965T>A | GRCh38 |
NC_000013.10:g.48923101T>A , CM000675.1:g.48923101T>A | GRCh37 |
NC_000013.9:g.47821102T>A | NCBI36 |
NG_009009.1:g.50219T>A , LRG_517:g.50219T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.549T>A MANE Select | ENSP00000267163.4:p.Thr183= | |
ENST00000650461.1:c.549T>A | ENSP00000497193.1:p.Thr183= | |
ENST00000267163.4:c.549T>A | ENSP00000267163.4:p.Thr183= | |
ENST00000467505.5:c.138-11052T>A | ENSP00000434702.1:n.138-11052T>A | |
ENST00000525036.1:n.711T>A | ||
NM_000321.2:c.549T>A , LRG_517t1:c.549T>A | NP_000312.2:p.Thr183= | |
XM_011535171.1:c.288T>A | XP_011533473.1:p.Thr96= | |
XM_011535171.2:c.288T>A | XP_011533473.1:p.Thr96= | |
NM_000321.3:c.549T>A MANE Select | NP_000312.2:p.Thr183= |