Linked Data
ClinVar Variation Id:
284323
dbSNP Id:
rs201796375
ExAC:
16:30997050 A / G
gnomAD v2:
16-30997050-A-G
gnomAD v3:
16-30985729-A-G
gnomAD v4:
16-30985729-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30985729A>G , CM000678.2:g.30985729A>G | GRCh38 |
| NC_000016.9:g.30997050A>G , CM000678.1:g.30997050A>G | GRCh37 |
| NC_000016.8:g.30904551A>G | NCBI36 |
| NG_012346.1:g.5532A>G | |
| NG_052948.1:g.33436A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297679.10:c.71A>G MANE Select | ENSP00000297679.5:p.His24Arg | |
| ENST00000262520.10:c.71A>G | ENSP00000262520.6:p.His24Arg | |
| ENST00000297679.9:c.71A>G | ENSP00000297679.5:p.His24Arg | |
| ENST00000562932.5:c.71A>G | ENSP00000459852.1:p.His24Arg | |
| ENST00000574447.1:c.71A>G | ENSP00000459689.1:p.His24Arg | |
| NM_001142777.1:c.71A>G | NP_001136249.1:p.His24Arg | |
| NM_001142778.1:c.71A>G | NP_001136250.1:p.His24Arg | |
| NM_025193.3:c.71A>G | NP_079469.2:p.His24Arg | |
| XM_005255601.3:c.71A>G | XP_005255658.2:p.His24Arg | |
| XM_011545960.1:c.71A>G | XP_011544262.1:p.His24Arg | |
| XM_011545961.1:c.71A>G | XP_011544263.1:p.His24Arg | |
| XM_011545962.1:c.71A>G | XP_011544264.1:p.His24Arg | |
| XM_011545960.2:c.71A>G | XP_011544262.1:p.His24Arg | |
| XM_011545962.2:c.71A>G | XP_011544264.1:p.His24Arg | |
| XM_017023732.1:c.71A>G | XP_016879221.1:p.His24Arg | |
| NM_025193.4:c.71A>G MANE Select | NP_079469.2:p.His24Arg | |
| NM_001142777.2:c.71A>G | NP_001136249.1:p.His24Arg | |
| NM_001142778.2:c.71A>G | NP_001136250.1:p.His24Arg |