Linked Data
ClinVar Variation Id:
370603
ClinVar RCV Id:
RCV003558360
dbSNP Id:
rs1057516622
gnomAD v4:
1-21575731-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.21575731A>G , CM000663.2:g.21575731A>G | GRCh38 |
| NC_000001.10:g.21902224A>G , CM000663.1:g.21902224A>G | GRCh37 |
| NC_000001.9:g.21774811A>G | NCBI36 |
| NG_008940.1:g.71367A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000374840.8:c.998-2A>G MANE Select | ENSP00000363973.3:n.998-2A>G | |
| ENST00000374829.2:n.267-2A>G | ||
| ENST00000374830.2:c.73-2A>G | ||
| ENST00000374832.5:c.998-2A>G | ENSP00000363965.1:n.998-2A>G | |
| ENST00000374840.7:c.998-2A>G | ENSP00000363973.3:n.998-2A>G | |
| ENST00000539907.5:c.767-2A>G | ENSP00000437674.1:n.767-2A>G | |
| ENST00000540617.5:c.833-2A>G | ENSP00000442672.1:n.833-2A>G | |
| NM_000478.4:c.998-2A>G | NP_000469.3:n.998-2A>G | |
| NM_001127501.2:c.833-2A>G | NP_001120973.2:n.833-2A>G | |
| NM_001177520.1:c.767-2A>G | NP_001170991.1:n.767-2A>G | |
| XM_005245818.1:c.998-2A>G | XP_005245875.1:n.998-2A>G | |
| XM_006710546.1:c.998-2A>G | XP_006710609.1:n.998-2A>G | |
| NM_000478.5:c.998-2A>G | NP_000469.3:n.998-2A>G | |
| NM_001127501.3:c.833-2A>G | NP_001120973.2:n.833-2A>G | |
| NM_001177520.2:c.767-2A>G | NP_001170991.1:n.767-2A>G | |
| XM_006710546.3:c.998-2A>G | XP_006710609.1:n.998-2A>G | |
| XM_017000903.1:c.842-2A>G | XP_016856392.1:n.842-2A>G | |
| NM_000478.6:c.998-2A>G MANE Select | NP_000469.3:n.998-2A>G | |
| NM_001127501.4:c.833-2A>G | NP_001120973.2:n.833-2A>G | |
| NM_001177520.3:c.767-2A>G | NP_001170991.1:n.767-2A>G | |
| NM_001369803.2:c.998-2A>G | NP_001356732.1:n.998-2A>G | |
| NM_001369804.2:c.998-2A>G | NP_001356733.1:n.998-2A>G | |
| NM_001369805.2:c.998-2A>G | NP_001356734.1:n.998-2A>G |