Linked Data
ClinVar Variation Id:
2562706
ClinVar RCV Id:
RCV003296699
MyVariant Identifiers:
chr1:g.161326622C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.161356832C>A , CM000663.2:g.161356832C>A | GRCh38 |
| NC_000001.10:g.161326622C>A , CM000663.1:g.161326622C>A | GRCh37 |
| NC_000001.9:g.159593246C>A | NCBI36 |
| NG_012767.1:g.47457C>A , LRG_317:g.47457C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470743.5:c.*398C>A | ENSP00000482902.2:n.*398C>A | |
| ENST00000367975.7:c.397C>A MANE Select | ENSP00000356953.3:p.Arg133= | |
| ENST00000342751.8:c.242-5497C>A | ENSP00000356952.3:n.242-5497C>A | |
| ENST00000367975.6:c.397C>A | ENSP00000356953.2:p.Arg133= | |
| ENST00000392169.6:c.238C>A | ENSP00000376009.2:p.Arg80= | |
| ENST00000432287.6:c.295C>A | ENSP00000390558.2:p.Arg99= | |
| ENST00000470743.4:c.495C>A | ||
| ENST00000504963.5:c.*220C>A | ENSP00000423929.1:n.*220C>A | |
| ENST00000513009.5:c.140-5497C>A | ENSP00000423260.1:n.140-5497C>A | |
| NM_001035511.1:c.242-5497C>A | NP_001030588.1:n.242-5497C>A | |
| NM_001035512.1:c.295C>A | NP_001030589.1:p.Arg99= | |
| NM_001035513.1:c.238C>A | NP_001030590.1:p.Arg80= | |
| NM_001278172.1:c.140-5497C>A | NP_001265101.1:n.140-5497C>A | |
| NM_003001.3:c.397C>A , LRG_317t1:c.397C>A | NP_002992.1:p.Arg133= | |
| NR_103459.1:n.454C>A | ||
| NM_001035511.2:c.242-5497C>A | NP_001030588.1:n.242-5497C>A | |
| NM_001035512.2:c.295C>A | NP_001030589.1:p.Arg99= | |
| NM_001035513.2:c.238C>A | NP_001030590.1:p.Arg80= | |
| NM_001278172.2:c.140-5497C>A | NP_001265101.1:n.140-5497C>A | |
| NM_003001.5:c.397C>A MANE Select | NP_002992.1:p.Arg133= | |
| NR_103459.2:n.449C>A |