Linked Data
ClinVar Variation Id:
2365216
ClinVar RCV Id:
RCV003000672
dbSNP Id:
rs1434116020
gnomAD v2:
4-88929372-C-A
gnomAD v4:
4-88008220-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.88008220C>A , CM000666.2:g.88008220C>A | GRCh38 |
| NC_000004.11:g.88929372C>A , CM000666.1:g.88929372C>A | GRCh37 |
| NC_000004.10:g.89148396C>A | NCBI36 |
| NG_008604.1:g.5553C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237596.7:c.487C>A MANE Select | ENSP00000237596.2:p.Pro163Thr | |
| ENST00000237596.6:c.487C>A | ENSP00000237596.2:p.Pro163Thr | |
| NM_000297.3:c.487C>A | NP_000288.1:p.Pro163Thr | |
| XM_011532028.1:c.487C>A | XP_011530330.1:p.Pro163Thr | |
| XR_244632.2:n.582C>A | ||
| NR_156488.1:n.574C>A | ||
| XM_011532028.2:c.487C>A | XP_011530330.1:p.Pro163Thr | |
| NM_000297.4:c.487C>A MANE Select | NP_000288.1:p.Pro163Thr | |
| NR_156488.2:n.586C>A |