Linked Data
ClinVar Variation Id:
455001
ClinVar RCV Id:
RCV000554590
dbSNP Id:
rs764066045
ExAC:
16:84208273 A / C
gnomAD v2:
16-84208273-A-C
gnomAD v4:
16-84174667-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.84174667A>C , CM000678.2:g.84174667A>C | GRCh38 |
| NC_000016.9:g.84208273A>C , CM000678.1:g.84208273A>C | GRCh37 |
| NC_000016.8:g.82765774A>C | NCBI36 |
| NG_021174.1:g.34409A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378553.10:c.1645-2A>C MANE Select | ENSP00000367815.5:n.1645-2A>C | |
| ENST00000378553.9:c.1645-2A>C | ENSP00000367815.5:n.1645-2A>C | |
| ENST00000563093.5:c.*200-2A>C | ENSP00000457373.1:n.*200-2A>C | |
| ENST00000563818.5:n.1322-2A>C | ||
| ENST00000570298.5:n.4090A>C | ||
| NM_178452.4:c.1645-2A>C | NP_848547.4:n.1645-2A>C | |
| XM_006721129.1:c.1645-2A>C | XP_006721192.1:n.1645-2A>C | |
| XM_011522850.1:c.1693-2A>C | XP_011521152.1:n.1693-2A>C | |
| XM_011522851.1:c.1693-2A>C | XP_011521153.1:n.1693-2A>C | |
| XM_011522852.1:c.1645-2A>C | XP_011521154.1:n.1645-2A>C | |
| XM_011522853.1:c.1693-2A>C | XP_011521155.1:n.1693-2A>C | |
| XM_011522854.1:c.1693-2A>C | XP_011521156.1:n.1693-2A>C | |
| XM_011522855.1:c.1693-2A>C | XP_011521157.1:n.1693-2A>C | |
| XM_011522856.1:c.1432-2A>C | XP_011521158.1:n.1432-2A>C | |
| XM_011522857.1:c.1693-2A>C | XP_011521159.1:n.1693-2A>C | |
| XM_011522858.1:c.1693-2A>C | XP_011521160.1:n.1693-2A>C | |
| XM_011522859.1:c.937-2A>C | XP_011521161.1:n.937-2A>C | |
| XM_011522860.1:c.937-2A>C | XP_011521162.1:n.937-2A>C | |
| NM_001318756.1:c.937-2A>C | NP_001305685.1:n.937-2A>C | |
| NM_178452.5:c.1645-2A>C | NP_848547.4:n.1645-2A>C | |
| XM_006721129.3:c.1645-2A>C | XP_006721192.1:n.1645-2A>C | |
| XM_011522853.3:c.1693-2A>C | XP_011521155.1:n.1693-2A>C | |
| XM_011522854.3:c.1693-2A>C | XP_011521156.1:n.1693-2A>C | |
| XM_011522855.3:c.1693-2A>C | XP_011521157.1:n.1693-2A>C | |
| XM_011522857.3:c.1693-2A>C | XP_011521159.1:n.1693-2A>C | |
| XM_011522858.3:c.1693-2A>C | XP_011521160.1:n.1693-2A>C | |
| XM_017022918.2:c.1645-2A>C | XP_016878407.1:n.1645-2A>C | |
| XM_017022919.1:c.1432-2A>C | XP_016878408.1:n.1432-2A>C | |
| XM_017022920.2:c.937-2A>C | XP_016878409.1:n.937-2A>C | |
| XM_017022921.2:c.889-2A>C | XP_016878410.1:n.889-2A>C | |
| XM_017022922.2:c.889-2A>C | XP_016878411.1:n.889-2A>C | |
| XR_001751829.2:n.1867-2A>C | ||
| XR_001751830.2:n.1867-2A>C | ||
| XR_001751831.2:n.1819-2A>C | ||
| XR_001751832.1:n.4419A>C | ||
| NM_178452.6:c.1645-2A>C MANE Select | NP_848547.4:n.1645-2A>C |