HGVS | Genome Assembly |
---|---|
NC_000011.10:g.112164736T= , CM000673.2:g.112164736T= | GRCh38 |
NC_000011.9:g.112035459T= , CM000673.1:g.112035459T= | GRCh37 |
NC_000011.8:g.111540669T= | NCBI36 |
NG_028143.1:g.4382A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000525987.5:n.320-5683T= | ||
ENST00000531744.5:c.315-5683T= | ENSP00000456957.1:n.315-5683T= | |
ENST00000532699.1:c.315-5683T= | ENSP00000456434.1:n.315-5683T= |