HGVS | Genome Assembly |
---|---|
NC_000006.12:g.26107224G>C , CM000668.2:g.26107224G>C | GRCh38 |
NC_000006.11:g.26107452G>C , CM000668.1:g.26107452G>C | GRCh37 |
NC_000006.10:g.26215431G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000707188.1:c.391-16190C>G (H2BC4) | ENSP00000516775.1:n.391-16190C>G | |
ENST00000629531.1:c.132+16549C>G (H2BC3) | ENSP00000486472.1:n.132+16549C>G |