Linked Data
ClinVar Variation Id:
2778911
ClinVar RCV Id:
RCV003663269
gnomAD v4:
10-49470609-T-C
MyVariant Identifiers:
chr10:g.50678655T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.49470609T>C , CM000672.2:g.49470609T>C | GRCh38 |
| NC_000010.10:g.50678655T>C , CM000672.1:g.50678655T>C | GRCh37 |
| NC_000010.9:g.50348661T>C | NCBI36 |
| NG_009442.1:g.73493A>G , LRG_465:g.73493A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355832.10:c.3351A>G MANE Select | ENSP00000348089.5:p.Pro1117= | |
| ENST00000679552.1:n.422A>G | ||
| ENST00000679871.1:n.497A>G | ||
| ENST00000679974.1:n.400A>G | ||
| ENST00000681632.1:n.4754A>G | ||
| ENST00000681659.1:c.3192A>G | ENSP00000505631.1:p.Pro1064= | |
| ENST00000355832.9:c.3351A>G | ENSP00000348089.5:p.Pro1117= | |
| ENST00000623073.3:c.*1647A>G | ENSP00000485650.1:n.*1647A>G | |
| ENST00000623115.3:c.1461A>G | ENSP00000485321.1:p.Pro487= | |
| ENST00000624341.3:c.1183A>G | ||
| NM_000124.3:c.3351A>G | NP_000115.1:p.Pro1117= | |
| XR_945953.1:n.243-956T>C | ||
| NM_001346440.1:c.3351A>G | NP_001333369.1:p.Pro1117= | |
| NM_000124.4:c.3351A>G MANE Select | NP_000115.1:p.Pro1117= | |
| NM_001346440.2:c.3351A>G | NP_001333369.1:p.Pro1117= |