Linked Data
ClinVar Variation Id:
1184616
ClinVar RCV Id:
RCV001542793
dbSNP Id:
rs751822337
gnomAD v4:
17-8015846-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8015846G>A , CM000679.2:g.8015846G>A | GRCh38 |
| NC_000017.10:g.7919164G>A , CM000679.1:g.7919164G>A | GRCh37 |
| NC_000017.9:g.7859889G>A | NCBI36 |
| NG_009092.1:g.18177G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254854.5:c.3043+5G>A MANE Select | ENSP00000254854.4:n.3043+5G>A | |
| ENST00000254854.4:c.3043+5G>A | ENSP00000254854.4:n.3043+5G>A | |
| NM_000180.3:c.3043+5G>A | NP_000171.1:n.3043+5G>A | |
| XM_011523816.1:c.3043+5G>A | XP_011522118.1:n.3043+5G>A | |
| NM_000180.4:c.3043+5G>A MANE Select | NP_000171.1:n.3043+5G>A |