HGVS | Genome Assembly |
---|---|
NC_000011.10:g.112164729T= , CM000673.2:g.112164729T= | GRCh38 |
NC_000011.9:g.112035452T= , CM000673.1:g.112035452T= | GRCh37 |
NC_000011.8:g.111540662T= | NCBI36 |
NG_028143.1:g.4389A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000525987.5:n.320-5690T= | ||
ENST00000531744.5:c.315-5690T= | ENSP00000456957.1:n.315-5690T= | |
ENST00000532699.1:c.315-5690T= | ENSP00000456434.1:n.315-5690T= |