HGVS | Genome Assembly |
---|---|
NC_000002.12:g.84425463T>A , CM000664.2:g.84425463T>A | GRCh38 |
NC_000002.11:g.84652587T>A , CM000664.1:g.84652587T>A | GRCh37 |
NC_000002.10:g.84506098T>A | NCBI36 |
NG_016755.1:g.39000A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393868.7:c.966A>T MANE Select | ENSP00000377446.2:p.Gly322= | |
ENST00000651342.1:c.*406A>T | ENSP00000498471.1:n.*406A>T | |
ENST00000393868.6:c.966A>T | ENSP00000377446.2:p.Gly322= | |
ENST00000484365.1:n.1474A>T | ||
ENST00000487809.1:n.713A>T | ||
ENST00000491123.5:n.812A>T | ||
NM_003849.3:c.966A>T | NP_003840.2:p.Gly322= | |
NM_003849.4:c.966A>T MANE Select | NP_003840.2:p.Gly322= |