Linked Data
ClinVar Variation Id:
1411559
ClinVar RCV Id:
RCV001918850
dbSNP Id:
rs1429465691
gnomAD v2:
1-160097351-G-A
gnomAD v3:
1-160127561-G-A
gnomAD v4:
1-160127561-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160127561G>A , CM000663.2:g.160127561G>A | GRCh38 |
| NC_000001.10:g.160097351G>A , CM000663.1:g.160097351G>A | GRCh37 |
| NC_000001.9:g.158363975G>A | NCBI36 |
| NG_008014.1:g.16804G>A , LRG_6:g.16804G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361216.8:c.758G>A MANE Select | ENSP00000354490.3:p.Arg253Lys | |
| ENST00000361216.7:c.758G>A | ENSP00000354490.3:p.Arg253Lys | |
| ENST00000392233.7:c.758G>A | ENSP00000376066.3:p.Arg253Lys | |
| ENST00000472488.5:n.861G>A | ||
| NM_000702.3:c.758G>A | NP_000693.1:p.Arg253Lys | |
| NM_000702.4:c.758G>A MANE Select | NP_000693.1:p.Arg253Lys |