Linked Data
ClinVar Variation Id:
2962616
ClinVar RCV Id:
RCV003827726
gnomAD v4:
5-33984521-G-A
MyVariant Identifiers:
chr5:g.33984626G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.33984521G>A , CM000667.2:g.33984521G>A | GRCh38 |
| NC_000005.9:g.33984626G>A , CM000667.1:g.33984626G>A | GRCh37 |
| NC_000005.8:g.34020383G>A | NCBI36 |
| NG_011691.2:g.5155C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296589.9:c.63C>T MANE Select | ENSP00000296589.4:p.Pro21= | |
| ENST00000296589.8:c.63C>T | ENSP00000296589.4:p.Pro21= | |
| ENST00000382102.7:c.63C>T | ENSP00000371534.3:p.Pro21= | |
| ENST00000505056.1:n.42C>T | ||
| ENST00000509381.1:c.63C>T | ENSP00000421100.1:p.Pro21= | |
| NM_001012509.3:c.63C>T | NP_001012527.1:p.Pro21= | |
| NM_001297417.2:c.63C>T | NP_001284346.2:p.Pro21= | |
| NM_016180.4:c.63C>T | NP_057264.3:p.Pro21= | |
| XM_011514052.1:c.63C>T | XP_011512354.1:p.Pro21= | |
| XR_925620.1:n.624C>T | ||
| NM_016180.5:c.63C>T MANE Select | NP_057264.4:p.Pro21= | |
| NM_001012509.4:c.63C>T | NP_001012527.2:p.Pro21= | |
| NM_001297417.3:c.63C>T | NP_001284346.2:p.Pro21= | |
| NM_001297417.4:c.63C>T | NP_001284346.2:p.Pro21= |