Linked Data
ClinVar Variation Id:
2947886
ClinVar RCV Id:
RCV003804516
MyVariant Identifiers:
chr1:g.68895498G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68429815G>A , CM000663.2:g.68429815G>A | GRCh38 |
| NC_000001.10:g.68895498G>A , CM000663.1:g.68895498G>A | GRCh37 |
| NC_000001.9:g.68668086G>A | NCBI36 |
| NG_008472.1:g.25145C>T | |
| NG_008472.2:g.25145C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1563C>T MANE Select | ENSP00000262340.5:p.Asn521= | |
| ENST00000262340.5:c.1563C>T | ENSP00000262340.5:p.Asn521= | |
| NM_000329.2:c.1563C>T | NP_000320.1:p.Asn521= | |
| XM_017002027.1:c.1287C>T | XP_016857516.1:p.Asn429= | |
| NM_000329.3:c.1563C>T MANE Select | NP_000320.1:p.Asn521= |