HGVS | Genome Assembly |
---|---|
NC_000006.12:g.26107211C>T , CM000668.2:g.26107211C>T | GRCh38 |
NC_000006.11:g.26107439C>T , CM000668.1:g.26107439C>T | GRCh37 |
NC_000006.10:g.26215418C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000707188.1:c.391-16177G>A (H2BC4) | ENSP00000516775.1:n.391-16177G>A | |
ENST00000629531.1:c.132+16562G>A (H2BC3) | ENSP00000486472.1:n.132+16562G>A |