HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48380232A>C , CM000675.2:g.48380232A>C | GRCh38 |
NC_000013.10:g.48954368A>C , CM000675.1:g.48954368A>C | GRCh37 |
NC_000013.9:g.47852369A>C | NCBI36 |
NG_009009.1:g.81486A>C , LRG_517:g.81486A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.1489A>C MANE Select | ENSP00000267163.4:p.Thr497Pro | |
ENST00000650461.1:c.1489A>C | ENSP00000497193.1:p.Thr497Pro | |
ENST00000267163.4:c.1489A>C | ENSP00000267163.4:p.Thr497Pro | |
NM_000321.2:c.1489A>C , LRG_517t1:c.1489A>C | NP_000312.2:p.Thr497Pro | |
XM_011535171.1:c.1228A>C | XP_011533473.1:p.Thr410Pro | |
XM_011535171.2:c.1228A>C | XP_011533473.1:p.Thr410Pro | |
NM_000321.3:c.1489A>C MANE Select | NP_000312.2:p.Thr497Pro |