Linked Data
ClinVar Variation Id:
2976238
ClinVar RCV Id:
RCV003836388
dbSNP Id:
rs1405105860
gnomAD v2:
21-45712184-G-A
gnomAD v4:
21-44292301-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44292301G>A , CM000683.2:g.44292301G>A | GRCh38 |
| NC_000021.8:g.45712184G>A , CM000683.1:g.45712184G>A | GRCh37 |
| NC_000021.7:g.44536612G>A | NCBI36 |
| NG_009556.1:g.11422G>A , LRG_18:g.11422G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000291582.6:c.996-1G>A MANE Select | ENSP00000291582.5:n.996-1G>A | |
| ENST00000291582.5:c.996-1G>A | ENSP00000291582.5:n.996-1G>A | |
| ENST00000337909.5:n.457-1G>A | ||
| ENST00000397994.8:n.457-1G>A | ||
| ENST00000527919.5:n.1726-1G>A | ||
| ENST00000530812.5:n.2743-1G>A | ||
| NM_000383.3:c.996-1G>A | NP_000374.1:n.996-1G>A | |
| XM_011529551.1:c.993-1G>A | XP_011527853.1:n.993-1G>A | |
| NM_000383.4:c.996-1G>A MANE Select | NP_000374.1:n.996-1G>A |