Linked Data
ClinVar Variation Id:
2929972
ClinVar RCV Id:
RCV003787330
gnomAD v4:
1-6470870-G-A
MyVariant Identifiers:
chr1:g.6530930G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.6470870G>A , CM000663.2:g.6470870G>A | GRCh38 |
| NC_000001.10:g.6530930G>A , CM000663.1:g.6530930G>A | GRCh37 |
| NC_000001.9:g.6453517G>A | NCBI36 |
| NG_007978.1:g.54140C>T , LRG_262:g.54140C>T | |
| NG_029910.1:g.326C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340850.10:c.1407C>T | ENSP00000344570.5:p.His469= | |
| ENST00000377728.8:c.1407C>T MANE Select | ENSP00000366957.3:p.His469= | |
| ENST00000377740.5:c.1407C>T | ENSP00000366969.4:p.His469= | |
| ENST00000377748.6:c.1581C>T | ENSP00000366977.2:p.His527= | |
| ENST00000400913.6:c.1407C>T | ENSP00000383704.1:p.His469= | |
| ENST00000400915.8:c.1518C>T | ENSP00000383706.4:p.His506= | |
| ENST00000489097.6:n.1883C>T | ||
| ENST00000535355.6:c.1614C>T | ENSP00000441445.1:p.His538= | |
| ENST00000537245.6:c.1518C>T | ENSP00000439625.2:p.His506= | |
| ENST00000673471.2:c.1704C>T | ENSP00000500749.1:p.His568= | |
| ENST00000674685.1:n.440C>T | ||
| ENST00000674790.1:c.*1619C>T | ENSP00000502815.1:n.*1619C>T | |
| ENST00000674943.1:n.69C>T | ||
| ENST00000675123.1:c.1407C>T | ENSP00000502132.1:p.His469= | |
| ENST00000675548.1:c.*1235C>T | ENSP00000502684.1:n.*1235C>T | |
| ENST00000675694.1:c.1407C>T | ENSP00000501925.1:p.His469= | |
| ENST00000340850.9:c.1407C>T | ENSP00000344570.5:p.His469= | |
| ENST00000377725.5:c.1407C>T | ENSP00000366954.1:p.His469= | |
| ENST00000377728.7:c.1407C>T | ENSP00000366957.3:p.His469= | |
| ENST00000377732.5:c.1518C>T | ENSP00000366961.1:p.His506= | |
| ENST00000377740.4:c.1638C>T | ENSP00000366969.3:p.His546= | |
| ENST00000377748.5:c.1638C>T | ENSP00000366977.1:p.His546= | |
| ENST00000400913.5:c.1407C>T | ENSP00000383704.1:p.His469= | |
| ENST00000400915.7:c.1575C>T | ENSP00000383706.3:p.His525= | |
| ENST00000487949.4:n.609C>T | ||
| ENST00000489097.5:n.1883C>T | ||
| ENST00000535355.5:c.1614C>T | ENSP00000441445.1:p.His538= | |
| ENST00000537245.5:c.1644C>T | ENSP00000439625.1:p.His548= | |
| NM_001042663.1:c.1575C>T | NP_001036128.1:p.His525= | |
| NM_001042664.1:c.1407C>T | NP_001036129.1:p.His469= | |
| NM_001042665.1:c.1407C>T | NP_001036130.1:p.His469= | |
| NM_001265592.1:c.1644C>T | NP_001252521.1:p.His548= | |
| NM_001265593.1:c.1614C>T | NP_001252522.1:p.His538= | |
| NM_001265594.1:c.1407C>T | NP_001252523.1:p.His469= | |
| NM_020631.4:c.1407C>T | NP_065682.2:p.His469= | |
| NM_198681.3:c.1638C>T | NP_941374.2:p.His546= | |
| NM_001042663.2:c.1575C>T | NP_001036128.1:p.His525= | |
| NM_001265594.2:c.1407C>T | NP_001252523.1:p.His469= | |
| NM_020631.5:c.1407C>T | NP_065682.2:p.His469= | |
| NM_001042663.3:c.1518C>T | NP_001036128.2:p.His506= | |
| NM_001265592.2:c.1518C>T | NP_001252521.2:p.His506= | |
| NM_020631.6:c.1407C>T MANE Select | NP_065682.2:p.His469= | |
| NM_198681.4:c.1407C>T | NP_941374.3:p.His469= |