Linked Data
ClinVar Variation Id:
384535
ClinVar RCV Id:
RCV000418672
dbSNP Id:
rs779468229
ExAC:
17:56769969 A / G
gnomAD v2:
17-56769969-A-G
gnomAD v3:
17-58692608-A-G
gnomAD v4:
17-58692608-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58692608A>G , CM000679.2:g.58692608A>G | GRCh38 |
| NC_000017.10:g.56769969A>G , CM000679.1:g.56769969A>G | GRCh37 |
| NC_000017.9:g.54124968A>G | NCBI36 |
| NG_023199.1:g.5007A>G , LRG_314:g.5007A>G | |
| NG_047169.1:g.4472T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461271.6:c.-284A>G | ENSP00000464056.2:n.-284A>G | |
| ENST00000697675.1:n.36A>G | ||
| ENST00000697676.1:n.25A>G | ||
| ENST00000697677.1:n.23A>G | ||
| ENST00000697678.1:n.23A>G | ||
| ENST00000697679.1:n.16A>G | ||
| ENST00000697680.1:c.-36A>G | ENSP00000513392.1:n.-36A>G | |
| ENST00000697681.1:c.-36A>G | ENSP00000513393.1:n.-36A>G | |
| ENST00000697683.1:c.-36A>G | ENSP00000513395.1:n.-36A>G | |
| ENST00000697684.1:n.25A>G | ||
| ENST00000697685.1:c.-36A>G | ENSP00000513396.1:n.-36A>G | |
| ENST00000697686.1:c.-231A>G | ENSP00000513397.1:n.-231A>G | |
| ENST00000697687.1:n.11A>G | ||
| ENST00000697688.1:n.11A>G | ||
| ENST00000697689.1:c.-36A>G | ENSP00000513398.1:n.-36A>G | |
| ENST00000697690.1:c.-36A>G | ENSP00000513399.1:n.-36A>G | |
| ENST00000337432.9:c.-36A>G MANE Select | ENSP00000336701.4:n.-36A>G | |
| ENST00000337432.8:c.-36A>G | ENSP00000336701.4:n.-36A>G | |
| ENST00000461271.5:c.-284A>G | ENSP00000464056.1:n.-284A>G | |
| ENST00000475762.5:c.-36A>G | ENSP00000432421.1:n.-36A>G | |
| ENST00000476741.2:n.7A>G | ||
| ENST00000486827.1:c.-36A>G | ENSP00000436761.1:n.-36A>G | |
| ENST00000487525.5:c.-36A>G | ENSP00000431637.1:n.-36A>G | |
| ENST00000487921.5:n.33A>G | ||
| ENST00000583539.5:c.-36A>G | ENSP00000463121.1:n.-36A>G | |
| NM_002876.3:c.-36A>G | NP_002867.1:n.-36A>G | |
| NM_058216.2:c.-36A>G | NP_478123.1:n.-36A>G | |
| NR_103872.1:n.36A>G | ||
| NR_103873.1:n.36A>G | ||
| XM_006722001.2:c.-36A>G | XP_006722064.1:n.-36A>G | |
| XM_006722002.2:c.-36A>G | XP_006722065.1:n.-36A>G | |
| XM_006722004.2:c.-284A>G | XP_006722067.1:n.-284A>G | |
| XM_006722005.2:c.-231A>G | XP_006722068.1:n.-231A>G | |
| XM_011525092.1:c.-584A>G | XP_011523394.1:n.-584A>G | |
| XM_011525093.1:c.-745A>G | XP_011523395.1:n.-745A>G | |
| XR_934513.1:n.38A>G | ||
| XR_934514.1:n.38A>G | ||
| XM_006722001.4:c.-36A>G | XP_006722064.1:n.-36A>G | |
| XM_006722002.4:c.-36A>G | XP_006722065.1:n.-36A>G | |
| XM_006722004.3:c.-284A>G | XP_006722067.1:n.-284A>G | |
| XM_006722005.3:c.-231A>G | XP_006722068.1:n.-231A>G | |
| XM_017024914.1:c.-284A>G | XP_016880403.1:n.-284A>G | |
| XM_017024917.1:c.-231A>G | XP_016880406.1:n.-231A>G | |
| XR_934513.3:n.469A>G | ||
| XR_934514.3:n.469A>G | ||
| NM_058216.3:c.-36A>G MANE Select | NP_478123.1:n.-36A>G | |
| NR_103872.2:n.7A>G | ||
| NM_002876.4:c.-36A>G | NP_002867.1:n.-36A>G |