Linked Data
ClinVar Variation Id:
3072603
ClinVar RCV Id:
RCV004013625
MyVariant Identifiers:
chr1:g.201044702C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.201075574C>T , CM000663.2:g.201075574C>T | GRCh38 |
| NC_000001.10:g.201044702C>T , CM000663.1:g.201044702C>T | GRCh37 |
| NC_000001.9:g.199311325C>T | NCBI36 |
| NG_009816.1:g.41993G>A | |
| NG_009816.2:g.41993G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362061.4:c.1869G>A MANE Select | ENSP00000355192.3:p.Gly623= | |
| ENST00000679417.1:c.*1032G>A | ENSP00000506706.1:n.*1032G>A | |
| ENST00000680059.1:c.1869G>A | ENSP00000504944.1:p.Gly623= | |
| ENST00000681078.1:c.1869G>A | ENSP00000506645.1:p.Gly623= | |
| ENST00000681190.1:c.1869G>A | ENSP00000506428.1:p.Gly623= | |
| ENST00000681874.1:c.1869G>A | ENSP00000505162.1:p.Gly623= | |
| ENST00000362061.3:c.1869G>A | ENSP00000355192.3:p.Gly623= | |
| ENST00000367338.7:c.1869G>A | ENSP00000356307.3:p.Gly623= | |
| NM_000069.2:c.1869G>A | NP_000060.2:p.Gly623= | |
| XM_005245478.2:c.1869G>A | XP_005245535.1:p.Gly623= | |
| XM_005245478.3:c.1869G>A | XP_005245535.1:p.Gly623= | |
| NM_000069.3:c.1869G>A MANE Select | NP_000060.2:p.Gly623= |