HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48537693G= , CM000677.2:g.48537693G= | GRCh38 |
NC_000015.9:g.48829890G= , CM000677.1:g.48829890G= | GRCh37 |
NC_000015.8:g.46617182G= | NCBI36 |
NG_008805.2:g.113096C= , LRG_778:g.113096C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.654C= | ENSP00000453958.2:p.Gly218= | |
ENST00000674301.2:c.654C= | ENSP00000501333.2:p.Gly218= | |
ENST00000316623.10:c.654C= MANE Select | ENSP00000325527.5:p.Gly218= | |
ENST00000316623.9:c.654C= | ENSP00000325527.5:p.Gly218= | |
ENST00000537463.6:c.636+18C= | ENSP00000440294.2:n.636+18C= | |
NM_000138.4:c.654C= , LRG_778t1:c.654C= | NP_000129.3:p.Gly218= | |
NM_000138.5:c.654C= MANE Select | NP_000129.3:p.Gly218= |