Linked Data
ClinVar Variation Id:
184117
dbSNP Id:
rs786201291
gnomAD v2:
5-112102884-A-G
gnomAD v4:
5-112767187-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112767187A>G , CM000667.2:g.112767187A>G | GRCh38 |
| NC_000005.9:g.112102884A>G , CM000667.1:g.112102884A>G | GRCh37 |
| NC_000005.8:g.112130783A>G | NCBI36 |
| NG_008481.4:g.79667A>G , LRG_130:g.79667A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.221-2A>G | ENSP00000484935.2:n.221-2A>G | |
| ENST00000504915.3:c.221-2A>G | ENSP00000473355.2:n.221-2A>G | |
| ENST00000505084.2:n.277-2A>G | ||
| ENST00000505350.2:c.*227-2A>G | ENSP00000481752.1:n.*227-2A>G | |
| ENST00000507379.6:c.251-2A>G | ENSP00000423224.2:n.251-2A>G | |
| ENST00000509732.6:c.221-2A>G | ENSP00000426541.2:n.221-2A>G | |
| ENST00000512211.7:c.221-2A>G | ENSP00000423828.3:n.221-2A>G | |
| ENST00000257430.9:c.221-2A>G MANE Select | ENSP00000257430.4:n.221-2A>G | |
| ENST00000257430.8:c.221-2A>G | ENSP00000257430.4:n.221-2A>G | |
| ENST00000507379.5:c.251-2A>G | ENSP00000423224.1:n.251-2A>G | |
| ENST00000508376.6:c.221-2A>G | ENSP00000427089.2:n.221-2A>G | |
| ENST00000508624.5:c.221-2A>G | ENSP00000424265.1:n.221-2A>G | |
| ENST00000509732.5:c.221-2A>G | ENSP00000426541.1:n.221-2A>G | |
| ENST00000512211.6:c.221-2A>G | ENSP00000423828.2:n.221-2A>G | |
| NM_000038.5:c.221-2A>G | NP_000029.2:n.221-2A>G | |
| NM_001127510.2:c.221-2A>G | NP_001120982.1:n.221-2A>G | |
| NM_001127511.2:c.251-2A>G | NP_001120983.2:n.251-2A>G | |
| NM_001354895.1:c.221-2A>G | NP_001341824.1:n.221-2A>G | |
| NM_001354896.1:c.221-2A>G | NP_001341825.1:n.221-2A>G | |
| NM_001354897.1:c.251-2A>G | NP_001341826.1:n.251-2A>G | |
| NM_001354898.1:c.146-2A>G | NP_001341827.1:n.146-2A>G | |
| NM_001354899.1:c.221-2A>G | NP_001341828.1:n.221-2A>G | |
| NM_001354900.1:c.44-2A>G | NP_001341829.1:n.44-2A>G | |
| NM_001354901.1:c.44-2A>G | NP_001341830.1:n.44-2A>G | |
| NM_001354902.1:c.251-2A>G | NP_001341831.1:n.251-2A>G | |
| NM_001354903.1:c.221-2A>G | NP_001341832.1:n.221-2A>G | |
| NM_001354904.1:c.146-2A>G | NP_001341833.1:n.146-2A>G | |
| NM_001354905.1:c.44-2A>G | NP_001341834.1:n.44-2A>G | |
| NM_001354906.1:c.-815-2A>G | NP_001341835.1:n.-815-2A>G | |
| NM_000038.6:c.221-2A>G MANE Select | NP_000029.2:n.221-2A>G | |
| NM_001127510.3:c.221-2A>G | NP_001120982.1:n.221-2A>G | |
| NM_001127511.3:c.251-2A>G | NP_001120983.2:n.251-2A>G | |
| NM_001354895.2:c.221-2A>G | NP_001341824.1:n.221-2A>G | |
| NM_001354896.2:c.221-2A>G | NP_001341825.1:n.221-2A>G | |
| NM_001354897.2:c.251-2A>G | NP_001341826.1:n.251-2A>G | |
| NM_001354898.2:c.146-2A>G | NP_001341827.1:n.146-2A>G | |
| NM_001354899.2:c.221-2A>G | NP_001341828.1:n.221-2A>G | |
| NM_001354900.2:c.44-2A>G | NP_001341829.1:n.44-2A>G | |
| NM_001354901.2:c.44-2A>G | NP_001341830.1:n.44-2A>G | |
| NM_001354902.2:c.251-2A>G | NP_001341831.1:n.251-2A>G | |
| NM_001354903.2:c.221-2A>G | NP_001341832.1:n.221-2A>G | |
| NM_001354904.2:c.146-2A>G | NP_001341833.1:n.146-2A>G | |
| NM_001354905.2:c.44-2A>G | NP_001341834.1:n.44-2A>G | |
| NM_001354906.2:c.-815-2A>G | NP_001341835.1:n.-815-2A>G |