Linked Data
dbSNP Id:
rs577352634
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81705644G>C , CM000665.2:g.81705644G>C | GRCh38 |
| NC_000003.11:g.81754795G>C , CM000665.1:g.81754795G>C | GRCh37 |
| NC_000003.10:g.81837485G>C | NCBI36 |
| NG_011810.1:g.61157C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.144-31C>G MANE Select | ENSP00000410833.2:n.144-31C>G | |
| ENST00000429644.6:c.144-31C>G | ENSP00000410833.2:n.144-31C>G | |
| ENST00000489715.1:c.21-31C>G | ENSP00000419638.1:n.21-31C>G | |
| NM_000158.3:c.144-31C>G | NP_000149.3:n.144-31C>G | |
| NM_000158.4:c.144-31C>G MANE Select | NP_000149.4:n.144-31C>G |