Linked Data
dbSNP Id:
rs993999318
gnomAD v2:
22-43558963-A-G
gnomAD v3:
22-43162957-A-G
gnomAD v4:
22-43162957-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43162957A>G , CM000684.2:g.43162957A>G | GRCh38 |
| NC_000022.10:g.43558963A>G , CM000684.1:g.43558963A>G | GRCh37 |
| NC_000022.9:g.41888907A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337554.8:c.476A>G MANE Select | ENSP00000338004.3:p.His159Arg | |
| ENST00000329563.8:c.476A>G | ENSP00000328973.4:p.His159Arg | |
| ENST00000337554.7:c.476A>G | ENSP00000338004.3:p.His159Arg | |
| ENST00000396265.4:c.476A>G | ENSP00000379563.4:p.His159Arg | |
| ENST00000583777.5:c.164A>G | ENSP00000463495.1:p.His55Arg | |
| NM_000714.5:c.476A>G | NP_000705.2:p.His159Arg | |
| NM_001256530.1:c.476A>G | NP_001243459.1:p.His159Arg | |
| NM_001256531.1:c.476A>G | NP_001243460.1:p.His159Arg | |
| NR_046308.1:n.385A>G | ||
| NM_000714.6:c.476A>G MANE Select | NP_000705.2:p.His159Arg | |
| NR_046308.2:n.340A>G |