Linked Data
ClinVar Variation Id:
942011
dbSNP Id:
rs1952051704
gnomAD v4:
13-48303931-C-A
MyVariant Identifiers:
chr13:g.48878067C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48303931C>A , CM000675.2:g.48303931C>A | GRCh38 |
| NC_000013.10:g.48878067C>A , CM000675.1:g.48878067C>A | GRCh37 |
| NC_000013.9:g.47776068C>A | NCBI36 |
| NG_009009.1:g.5185C>A , LRG_517:g.5185C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.19C>A MANE Select | ENSP00000267163.4:p.Arg7= | |
| ENST00000646097.1:c.19C>A | ENSP00000496556.1:p.Arg7= | |
| ENST00000650461.1:c.19C>A | ENSP00000497193.1:p.Arg7= | |
| ENST00000267163.4:c.19C>A | ENSP00000267163.4:p.Arg7= | |
| ENST00000467505.5:c.19C>A | ENSP00000434702.1:p.Arg7= | |
| ENST00000525036.1:n.181C>A | ||
| NM_000321.2:c.19C>A , LRG_517t1:c.19C>A | NP_000312.2:p.Arg7= | |
| NM_000321.3:c.19C>A MANE Select | NP_000312.2:p.Arg7= |