HGVS | Genome Assembly |
---|---|
NC_000022.11:g.49913625G= , CM000684.2:g.49913625G= | GRCh38 |
NC_000022.10:g.50307273G= , CM000684.1:g.50307273G= | GRCh37 |
NC_000022.9:g.48693277G= | NCBI36 |
NG_008927.1:g.9834C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330817.11:c.141C= MANE Select | ENSP00000333813.5:p.Tyr47= | |
ENST00000330817.10:c.141C= | ENSP00000333813.5:p.Tyr47= | |
NM_024105.3:c.141C= | NP_077010.1:p.Tyr47= | |
XM_011530369.1:c.141C= | XP_011528671.1:p.Tyr47= | |
XM_011530370.1:c.141C= | XP_011528672.1:p.Tyr47= | |
XM_011530371.1:c.141C= | XP_011528673.1:p.Tyr47= | |
XM_011530371.2:c.141C= | XP_011528673.1:p.Tyr47= | |
XM_017028936.1:c.141C= | XP_016884425.1:p.Tyr47= | |
XM_017028937.1:c.141C= | XP_016884426.1:p.Tyr47= | |
NM_024105.4:c.141C= MANE Select | NP_077010.1:p.Tyr47= |