HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154904945C>A , CM000685.2:g.154904945C>A | GRCh38 |
NC_000023.10:g.154133220C>A , CM000685.1:g.154133220C>A | GRCh37 |
NC_000023.9:g.153786414C>A | NCBI36 |
NG_011403.1:g.122779G>T | |
NG_011403.2:g.122779G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5452G>T MANE Select | ENSP00000353393.4:p.Gly1818Ter | |
ENST00000360256.8:c.5452G>T | ENSP00000353393.4:p.Gly1818Ter | |
NM_000132.3:c.5452G>T | NP_000123.1:p.Gly1818Ter | |
XM_011531126.1:c.5347G>T | XP_011529428.1:p.Gly1783Ter | |
NM_000132.4:c.5452G>T MANE Select | NP_000123.1:p.Gly1818Ter |