Linked Data
gnomAD v4:
3-81705521-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.81705521T>C , CM000665.2:g.81705521T>C | GRCh38 |
| NC_000003.11:g.81754672T>C , CM000665.1:g.81754672T>C | GRCh37 |
| NC_000003.10:g.81837362T>C | NCBI36 |
| NG_011810.1:g.61280A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429644.7:c.236A>G MANE Select | ENSP00000410833.2:p.His79Arg | |
| ENST00000429644.6:c.236A>G | ENSP00000410833.2:p.His79Arg | |
| ENST00000489715.1:c.113A>G | ENSP00000419638.1:p.His38Arg | |
| NM_000158.3:c.236A>G | NP_000149.3:p.His79Arg | |
| NM_000158.4:c.236A>G MANE Select | NP_000149.4:p.His79Arg |