Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.26107248T>C , CM000668.2:g.26107248T>C | GRCh38 |
| NC_000006.11:g.26107476T>C , CM000668.1:g.26107476T>C | GRCh37 |
| NC_000006.10:g.26215455T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000707188.1:c.391-16214A>G (H2BC4) | ENSP00000516775.1:n.391-16214A>G | |
| ENST00000629531.1:c.132+16525A>G (H2BC3) | ENSP00000486472.1:n.132+16525A>G |