Linked Data
ClinVar Variation Id:
2882337
ClinVar RCV Id:
RCV003600280
MyVariant Identifiers:
chr1:g.45966031G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45500359G>A , CM000663.2:g.45500359G>A | GRCh38 |
| NC_000001.10:g.45966031G>A , CM000663.1:g.45966031G>A | GRCh37 |
| NC_000001.9:g.45738618G>A | NCBI36 |
| NG_013378.1:g.5176G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000401061.9:c.27G>A MANE Select | ENSP00000383840.4:p.Lys9= | |
| ENST00000401061.8:c.27G>A | ENSP00000383840.4:p.Lys9= | |
| ENST00000616135.1:c.-145G>A | ENSP00000478859.1:n.-145G>A | |
| NM_015506.2:c.27G>A | NP_056321.2:p.Lys9= | |
| XM_005270724.3:c.27G>A | XP_005270781.1:p.Lys9= | |
| XM_011541204.1:c.-196G>A | XP_011539506.1:n.-196G>A | |
| NM_001330540.1:c.-196G>A | NP_001317469.1:n.-196G>A | |
| XM_005270724.5:c.27G>A | XP_005270781.1:p.Lys9= | |
| NM_015506.3:c.27G>A MANE Select | NP_056321.2:p.Lys9= | |
| NM_001330540.2:c.-196G>A | NP_001317469.1:n.-196G>A |