HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48463978T>G , CM000677.2:g.48463978T>G | GRCh38 |
NC_000015.9:g.48756175T>G , CM000677.1:g.48756175T>G | GRCh37 |
NC_000015.8:g.46543467T>G | NCBI36 |
NG_008805.2:g.186811A>C , LRG_778:g.186811A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000559133.6:c.4986A>C | ENSP00000453958.2:p.Thr1662= | |
ENST00000674301.2:c.4986A>C | ENSP00000501333.2:p.Thr1662= | |
ENST00000684448.1:n.3660A>C | ||
ENST00000316623.10:c.4986A>C MANE Select | ENSP00000325527.5:p.Thr1662= | |
ENST00000316623.9:c.4986A>C | ENSP00000325527.5:p.Thr1662= | |
ENST00000537463.6:c.*749A>C | ENSP00000440294.2:n.*749A>C | |
ENST00000559133.5:c.293A>C | ||
NM_000138.4:c.4986A>C , LRG_778t1:c.4986A>C | NP_000129.3:p.Thr1662= | |
NM_000138.5:c.4986A>C MANE Select | NP_000129.3:p.Thr1662= |