HGVS | Genome Assembly |
---|---|
NC_000006.12:g.26107219C= , CM000668.2:g.26107219C= | GRCh38 |
NC_000006.11:g.26107447C= , CM000668.1:g.26107447C= | GRCh37 |
NC_000006.10:g.26215426C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000707188.1:c.391-16185G= (H2BC4) | ENSP00000516775.1:n.391-16185G= | |
ENST00000629531.1:c.132+16554G= (H2BC3) | ENSP00000486472.1:n.132+16554G= |