Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816272C>G , CM000681.2:g.4816272C>G | GRCh38 |
| NC_000019.9:g.4816284C>G , CM000681.1:g.4816284C>G | GRCh37 |
| NC_000019.8:g.4767284C>G | NCBI36 |
| NG_031998.1:g.20471G>C , LRG_358:g.20471G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.2106G>C MANE Select | ENSP00000248244.4:p.Gln702His | |
| ENST00000248244.5:c.2106G>C | ENSP00000248244.4:p.Gln702His | |
| ENST00000621756.1:c.1608G>C | ENSP00000479467.1:p.Gln536His | |
| NM_182919.3:c.2106G>C , LRG_358t1:c.2106G>C | NP_891549.1:p.Gln702His | |
| NM_001385678.1:c.2064G>C | NP_001372607.1:p.Gln688His | |
| NM_001385679.1:c.1971G>C | NP_001372608.1:p.Gln657His | |
| NM_001385680.1:c.1464G>C | NP_001372609.1:p.Gln488His | |
| NM_182919.4:c.2106G>C MANE Select | NP_891549.1:p.Gln702His |