HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48468507G= , CM000677.2:g.48468507G= | GRCh38 |
NC_000015.9:g.48760704G= , CM000677.1:g.48760704G= | GRCh37 |
NC_000015.8:g.46547996G= | NCBI36 |
NG_008805.2:g.182282C= , LRG_778:g.182282C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.4487C= | ENSP00000453958.2:p.Thr1496= | |
ENST00000674301.2:c.4487C= | ENSP00000501333.2:p.Thr1496= | |
ENST00000684448.1:n.3161C= | ||
ENST00000316623.10:c.4487C= MANE Select | ENSP00000325527.5:p.Thr1496= | |
ENST00000316623.9:c.4487C= | ENSP00000325527.5:p.Thr1496= | |
ENST00000537463.6:c.*250C= | ENSP00000440294.2:n.*250C= | |
NM_000138.4:c.4487C= , LRG_778t1:c.4487C= | NP_000129.3:p.Thr1496= | |
NM_000138.5:c.4487C= MANE Select | NP_000129.3:p.Thr1496= |