ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8015048C>G , CM000679.2:g.8015048C>G | GRCh38 |
| NC_000017.10:g.7918366C>G , CM000679.1:g.7918366C>G | GRCh37 |
| NC_000017.9:g.7859091C>G | NCBI36 |
| NG_009092.1:g.17379C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254854.5:c.2766C>G MANE Select | ENSP00000254854.4:p.Tyr922Ter | |
| ENST00000254854.4:c.2766C>G | ENSP00000254854.4:p.Tyr922Ter | |
| NM_000180.3:c.2766C>G | NP_000171.1:p.Tyr922Ter | |
| XM_011523816.1:c.2766C>G | XP_011522118.1:p.Tyr922Ter | |
| NM_000180.4:c.2766C>G MANE Select | NP_000171.1:p.Tyr922Ter |