Linked Data
gnomAD v4:
19-4816597-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816597T>C , CM000681.2:g.4816597T>C | GRCh38 |
| NC_000019.9:g.4816609T>C , CM000681.1:g.4816609T>C | GRCh37 |
| NC_000019.8:g.4767609T>C | NCBI36 |
| NG_031998.1:g.20146A>G , LRG_358:g.20146A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.1781A>G MANE Select | ENSP00000248244.4:p.His594Arg | |
| ENST00000248244.5:c.1781A>G | ENSP00000248244.4:p.His594Arg | |
| ENST00000621756.1:c.1364A>G | ENSP00000479467.1:p.His455Arg | |
| NM_182919.3:c.1781A>G , LRG_358t1:c.1781A>G | NP_891549.1:p.His594Arg | |
| NM_001385678.1:c.1739A>G | NP_001372607.1:p.His580Arg | |
| NM_001385679.1:c.1646A>G | NP_001372608.1:p.His549Arg | |
| NM_001385680.1:c.1139A>G | NP_001372609.1:p.His380Arg | |
| NM_182919.4:c.1781A>G MANE Select | NP_891549.1:p.His594Arg |