Linked Data
ClinVar Variation Id:
2952454
ClinVar RCV Id:
RCV003815605
gnomAD v4:
22-18078517-G-C
MyVariant Identifiers:
chr22:g.18561283G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.18078517G>C , CM000684.2:g.18078517G>C | GRCh38 |
| NC_000022.10:g.18561283G>C , CM000684.1:g.18561283G>C | GRCh37 |
| NC_000022.9:g.16941283G>C | NCBI36 |
| NG_008339.1:g.5598G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399744.8:c.141G>C MANE Select | ENSP00000382648.4:p.Val47= | |
| ENST00000474897.6:c.141G>C | ENSP00000434235.2:p.Val47= | |
| ENST00000329627.11:c.141G>C | ENSP00000331106.5:p.Val47= | |
| ENST00000399744.7:c.141G>C | ENSP00000382648.3:p.Val47= | |
| ENST00000428061.2:c.141G>C | ENSP00000412441.2:p.Val47= | |
| ENST00000474897.5:c.141G>C | ENSP00000434235.1:p.Val47= | |
| ENST00000610387.4:c.141G>C | ENSP00000482091.1:p.Val47= | |
| NM_001127649.2:c.141G>C | NP_001121121.1:p.Val47= | |
| NM_001199319.1:c.141G>C | NP_001186248.1:p.Val47= | |
| NM_017929.5:c.141G>C | NP_060399.1:p.Val47= | |
| NM_001127649.3:c.141G>C MANE Select | NP_001121121.1:p.Val47= | |
| NM_001199319.2:c.141G>C | NP_001186248.1:p.Val47= | |
| NM_017929.6:c.141G>C | NP_060399.1:p.Val47= |