Linked Data
MyVariant Identifiers:
chr22:g.51135981C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50697553C>G , CM000684.2:g.50697553C>G | GRCh38 |
| NC_000022.10:g.51135981C>G , CM000684.1:g.51135981C>G | GRCh37 |
| NC_000022.9:g.49482847C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262795.7:c.948-11C>G | ENSP00000489147.2:n.948-11C>G | |
| ENST00000414786.7:n.1532-11C>G | ||
| ENST00000673971.2:c.1305-11C>G | ENSP00000501192.1:n.1305-11C>G | |
| ENST00000262795.6:c.948-11C>G | ENSP00000489147.2:n.948-11C>G | |
| ENST00000673971.1:c.1305-11C>G | ENSP00000501192.1:n.1305-11C>G | |
| ENST00000262795.5:c.1345-12C>G | ENSP00000489147.1:n.1345-12C>G | |
| ENST00000414786.6:n.1532-11C>G | ||
| ENST00000445220.5:c.1326-11C>G | ENSP00000489407.1:n.1326-11C>G |