Linked Data
gnomAD v4:
2-135789702-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135789702T>C , CM000664.2:g.135789702T>C | GRCh38 |
| NC_000002.11:g.136547272T>C , CM000664.1:g.136547272T>C | GRCh37 |
| NC_000002.10:g.136263742T>C | NCBI36 |
| NG_008104.2:g.70468A>G , LRG_338:g.70468A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264162.7:c.5432A>G MANE Select | ENSP00000264162.2:p.His1811Arg | |
| ENST00000264162.6:c.5432A>G | ENSP00000264162.2:p.His1811Arg | |
| NM_002299.2:c.5432A>G , LRG_338t1:c.5432A>G | NP_002290.2:p.His1811Arg | |
| NM_002299.3:c.5432A>G | NP_002290.2:p.His1811Arg | |
| NM_002299.4:c.5432A>G MANE Select | NP_002290.2:p.His1811Arg |