HGVS | Genome Assembly |
---|---|
NC_000003.12:g.81646511T= , CM000665.2:g.81646511T= | GRCh38 |
NC_000003.11:g.81695662T= , CM000665.1:g.81695662T= | GRCh37 |
NC_000003.10:g.81778352T= | NCBI36 |
NG_011810.1:g.120290A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000429644.7:c.692-29A= MANE Select | ENSP00000410833.2:n.692-29A= | |
ENST00000429644.6:c.692-29A= | ENSP00000410833.2:n.692-29A= | |
ENST00000489715.1:c.569-29A= | ENSP00000419638.1:n.569-29A= | |
ENST00000498468.1:n.220-7A= | ||
NM_000158.3:c.692-29A= | NP_000149.3:n.692-29A= | |
NM_000158.4:c.692-29A= MANE Select | NP_000149.4:n.692-29A= |