HGVS | Genome Assembly |
---|---|
NC_000008.11:g.10622546A= , CM000670.2:g.10622546A= | GRCh38 |
NC_000008.10:g.10480056A= , CM000670.1:g.10480056A= | GRCh37 |
NC_000008.9:g.10517466A= | NCBI36 |
NG_028035.1:g.37562T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382483.4:c.609+47T= MANE Select | ENSP00000371923.3:n.609+47T= | |
ENST00000329335.3:n.859+47T= | ||
ENST00000382483.3:c.609+47T= | ENSP00000371923.3:n.609+47T= | |
NM_178857.5:c.609+47T= | NP_849188.4:n.609+47T= | |
NM_178857.6:c.609+47T= MANE Select | NP_849188.4:n.609+47T= |