Linked Data
ClinVar Variation Id:
281735
dbSNP Id:
rs886042226
gnomAD v2:
9-103059234-A-G
gnomAD v3:
9-100296952-A-G
gnomAD v4:
9-100296952-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.100296952A>G , CM000671.2:g.100296952A>G | GRCh38 |
| NC_000009.11:g.103059234A>G , CM000671.1:g.103059234A>G | GRCh37 |
| NC_000009.10:g.102099055A>G | NCBI36 |
| NG_008316.1:g.202724A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262457.7:c.2822A>G MANE Select | ENSP00000262457.2:p.His941Arg | |
| ENST00000262456.6:c.2312A>G | ENSP00000262456.2:p.His771Arg | |
| ENST00000262457.6:c.2822A>G | ENSP00000262457.2:p.His941Arg | |
| NM_014425.3:c.2822A>G | NP_055240.2:p.His941Arg | |
| NM_183245.2:c.2312A>G | NP_899068.1:p.His771Arg | |
| NR_051962.1:n.3131A>G | ||
| XM_005251923.3:c.2822A>G | XP_005251980.1:p.His941Arg | |
| XM_005251924.3:c.2534A>G | XP_005251981.1:p.His845Arg | |
| XM_011518531.1:c.2822A>G | XP_011516833.1:p.His941Arg | |
| XM_011518532.1:c.2822A>G | XP_011516834.1:p.His941Arg | |
| XM_011518533.1:c.2822A>G | XP_011516835.1:p.His941Arg | |
| XM_011518534.1:c.2534A>G | XP_011516836.1:p.His845Arg | |
| XM_011518535.1:c.2534A>G | XP_011516837.1:p.His845Arg | |
| XM_011518536.1:c.2534A>G | XP_011516838.1:p.His845Arg | |
| XM_011518537.1:c.2534A>G | XP_011516839.1:p.His845Arg | |
| XM_011518538.1:c.2534A>G | XP_011516840.1:p.His845Arg | |
| XM_011518539.1:c.2501A>G | XP_011516841.1:p.His834Arg | |
| XM_011518540.1:c.2501A>G | XP_011516842.1:p.His834Arg | |
| XM_011518541.1:c.2501A>G | XP_011516843.1:p.His834Arg | |
| XM_011518542.1:c.2024A>G | XP_011516844.1:p.His675Arg | |
| XM_011518543.1:c.1844A>G | XP_011516845.1:p.His615Arg | |
| XM_011518544.1:c.1844A>G | XP_011516846.1:p.His615Arg | |
| XR_242585.1:n.3005A>G | ||
| XR_242586.1:n.3029A>G | ||
| XR_428522.1:n.2519A>G | ||
| NM_001318381.1:c.2534A>G | NP_001305310.1:p.His845Arg | |
| NM_001318382.1:c.1844A>G | NP_001305311.1:p.His615Arg | |
| NM_014425.4:c.2822A>G | NP_055240.2:p.His941Arg | |
| NR_134606.1:n.3029A>G | ||
| NM_014425.5:c.2822A>G MANE Select | NP_055240.2:p.His941Arg | |
| NM_001318381.2:c.2534A>G | NP_001305310.1:p.His845Arg | |
| NM_001318382.2:c.1844A>G | NP_001305311.1:p.His615Arg | |
| NR_134606.2:n.2971A>G |