HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15540656C= , CM000681.2:g.15540656C= | GRCh38 |
NC_000019.9:g.15651467C= , CM000681.1:g.15651467C= | GRCh37 |
NC_000019.8:g.15512467C= | NCBI36 |
NG_007987.1:g.37132C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269703.8:c.878C= MANE Select | ENSP00000269703.1:p.Ala293= | |
ENST00000269703.7:c.878C= | ENSP00000269703.1:p.Ala293= | |
ENST00000601005.2:c.878C= | ENSP00000469866.1:p.Ala293= | |
NM_173483.3:c.878C= | NP_775754.2:p.Ala293= | |
XM_011527692.1:c.878C= | XP_011525994.1:p.Ala293= | |
XM_011527693.1:c.878C= | XP_011525995.1:p.Ala293= | |
XM_011527692.2:c.878C= | XP_011525994.1:p.Ala293= | |
XM_011527693.2:c.878C= | XP_011525995.1:p.Ala293= | |
NM_173483.4:c.878C= MANE Select | NP_775754.2:p.Ala293= |