Linked Data
ClinVar Variation Id:
338277
ClinVar RCV Id:
RCV000330506
dbSNP Id:
rs375253690
ExAC:
20:32880153 G / A
gnomAD v2:
20-32880153-G-A
gnomAD v3:
20-34292347-G-A
gnomAD v4:
20-34292347-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.34292347G>A , CM000682.2:g.34292347G>A | GRCh38 |
| NC_000020.10:g.32880153G>A , CM000682.1:g.32880153G>A | GRCh37 |
| NC_000020.9:g.32343814G>A | NCBI36 |
| NG_012630.1:g.24456C>T | |
| NG_012630.2:g.24456C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217426.7:c.445+11C>T MANE Select | ENSP00000217426.2:n.445+11C>T | |
| ENST00000217426.6:c.445+11C>T | ENSP00000217426.2:n.445+11C>T | |
| ENST00000468908.1:n.608+11C>T | ||
| ENST00000480653.5:n.492+11C>T | ||
| ENST00000538132.1:c.361+11C>T | ENSP00000442820.1:n.361+11C>T | |
| NM_000687.2:c.445+11C>T | NP_000678.1:n.445+11C>T | |
| NM_001161766.1:c.361+11C>T | NP_001155238.1:n.361+11C>T | |
| XM_005260316.3:c.361+11C>T | XP_005260373.1:n.361+11C>T | |
| XM_005260317.1:c.361+11C>T | XP_005260374.1:n.361+11C>T | |
| XM_011528656.1:c.361+11C>T | XP_011526958.1:n.361+11C>T | |
| XM_011528657.1:c.361+11C>T | XP_011526959.1:n.361+11C>T | |
| XM_011528658.1:c.361+11C>T | XP_011526960.1:n.361+11C>T | |
| XM_011528659.1:c.361+11C>T | XP_011526961.1:n.361+11C>T | |
| XM_011528660.1:c.361+11C>T | XP_011526962.1:n.361+11C>T | |
| NM_000687.3:c.445+11C>T | NP_000678.1:n.445+11C>T | |
| NM_001322084.1:c.361+11C>T | NP_001309013.1:n.361+11C>T | |
| NM_001322085.1:c.361+11C>T | NP_001309014.1:n.361+11C>T | |
| NM_001322086.1:c.451+11C>T | NP_001309015.1:n.451+11C>T | |
| NM_001362750.1:c.445+11C>T | NP_001349679.1:n.445+11C>T | |
| XM_005260317.2:c.361+11C>T | XP_005260374.1:n.361+11C>T | |
| XM_011528656.3:c.451+11C>T | XP_011526958.2:n.451+11C>T | |
| XM_011528657.2:c.451+11C>T | XP_011526959.2:n.451+11C>T | |
| XM_011528658.3:c.451+11C>T | XP_011526960.2:n.451+11C>T | |
| XM_017027709.2:c.445+11C>T | XP_016883198.1:n.445+11C>T | |
| XM_017027710.2:c.67+11C>T | XP_016883199.1:n.67+11C>T | |
| NM_000687.4:c.445+11C>T MANE Select | NP_000678.1:n.445+11C>T | |
| NM_001322084.2:c.361+11C>T | NP_001309013.1:n.361+11C>T | |
| NM_001322085.2:c.361+11C>T | NP_001309014.1:n.361+11C>T | |
| NM_001322086.2:c.451+11C>T | NP_001309015.1:n.451+11C>T | |
| NM_001362750.2:c.445+11C>T | NP_001349679.1:n.445+11C>T | |
| NM_001161766.2:c.361+11C>T | NP_001155238.1:n.361+11C>T |