HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1014237T= , CM000663.2:g.1014237T= | GRCh38 |
NC_000001.10:g.949617T= , CM000663.1:g.949617T= | GRCh37 |
NC_000001.9:g.939480T= | NCBI36 |
NG_033033.1:g.5771T= | |
NG_033033.2:g.18100T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000624697.4:c.233T= | ENSP00000485643.1:p.Val78= | |
ENST00000649529.1:c.257T= MANE Select | ENSP00000496832.1:p.Val86= | |
ENST00000379389.4:c.257T= | ENSP00000368699.4:p.Val86= | |
ENST00000624652.1:c.233T= | ENSP00000485313.1:p.Val78= | |
ENST00000624697.3:c.233T= | ENSP00000485643.1:p.Val78= | |
NM_005101.3:c.257T= | NP_005092.1:p.Val86= | |
NM_005101.4:c.257T= MANE Select | NP_005092.1:p.Val86= |