HGVS | Genome Assembly |
---|---|
NC_000011.10:g.112164722A>C , CM000673.2:g.112164722A>C | GRCh38 |
NC_000011.9:g.112035445A>C , CM000673.1:g.112035445A>C | GRCh37 |
NC_000011.8:g.111540655A>C | NCBI36 |
NG_028143.1:g.4396T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000525987.5:n.320-5697A>C | ||
ENST00000531744.5:c.315-5697A>C | ENSP00000456957.1:n.315-5697A>C | |
ENST00000532699.1:c.315-5697A>C | ENSP00000456434.1:n.315-5697A>C |