HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48610771A>C , CM000677.2:g.48610771A>C | GRCh38 |
NC_000015.9:g.48902968A>C , CM000677.1:g.48902968A>C | GRCh37 |
NC_000015.8:g.46690260A>C | NCBI36 |
NG_008805.2:g.40018T>G , LRG_778:g.40018T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.303T>G | ENSP00000453958.2:p.Thr101= | |
ENST00000674301.2:c.303T>G | ENSP00000501333.2:p.Thr101= | |
ENST00000316623.10:c.303T>G MANE Select | ENSP00000325527.5:p.Thr101= | |
ENST00000316623.9:c.303T>G | ENSP00000325527.5:p.Thr101= | |
ENST00000537463.6:c.303T>G | ENSP00000440294.2:p.Thr101= | |
NM_000138.4:c.303T>G , LRG_778t1:c.303T>G | NP_000129.3:p.Thr101= | |
NM_000138.5:c.303T>G MANE Select | NP_000129.3:p.Thr101= |