Linked Data
dbSNP Id:
rs770060951
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.26107136G>T , CM000668.2:g.26107136G>T | GRCh38 |
| NC_000006.11:g.26107364G>T , CM000668.1:g.26107364G>T | GRCh37 |
| NC_000006.10:g.26215343G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000707188.1:c.391-16102C>A (H2BC4) | ENSP00000516775.1:n.391-16102C>A | |
| ENST00000629531.1:c.132+16637C>A (H2BC3) | ENSP00000486472.1:n.132+16637C>A |