Linked Data
ClinVar Variation Id:
127302
ClinVar RCV Id:
RCV000120016
RCV000115100
RCV000210376
RCV000587987
RCV000735965
RCV001353642
RCV003323290
dbSNP Id:
rs370560998
ExAC:
5:112176317 A / G
gnomAD v2:
5-112176317-A-G
gnomAD v3:
5-112840620-A-G
gnomAD v4:
5-112840620-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112840620A>G , CM000667.2:g.112840620A>G | GRCh38 |
| NC_000005.9:g.112176317A>G , CM000667.1:g.112176317A>G | GRCh37 |
| NC_000005.8:g.112204216A>G | NCBI36 |
| NG_008481.4:g.153100A>G , LRG_130:g.153100A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.5080A>G | ENSP00000473355.2:p.Arg1694Gly | |
| ENST00000505350.2:c.*5032A>G | ENSP00000481752.1:n.*5032A>G | |
| ENST00000507379.6:c.4972A>G | ENSP00000423224.2:p.Arg1658Gly | |
| ENST00000509732.6:c.5026A>G | ENSP00000426541.2:p.Arg1676Gly | |
| ENST00000512211.7:c.5026A>G | ENSP00000423828.3:p.Arg1676Gly | |
| ENST00000257430.9:c.5026A>G MANE Select | ENSP00000257430.4:p.Arg1676Gly | |
| ENST00000257430.8:c.5026A>G | ENSP00000257430.4:p.Arg1676Gly | |
| ENST00000508376.6:c.5026A>G | ENSP00000427089.2:p.Arg1676Gly | |
| ENST00000508624.5:c.*4348A>G | ENSP00000424265.1:n.*4348A>G | |
| ENST00000520401.1:c.230+11648A>G | ||
| NM_000038.5:c.5026A>G | NP_000029.2:p.Arg1676Gly | |
| NM_001127510.2:c.5026A>G | NP_001120982.1:p.Arg1676Gly | |
| NM_001127511.2:c.4972A>G | NP_001120983.2:p.Arg1658Gly | |
| NM_001354895.1:c.5026A>G | NP_001341824.1:p.Arg1676Gly | |
| NM_001354896.1:c.5080A>G | NP_001341825.1:p.Arg1694Gly | |
| NM_001354897.1:c.5056A>G | NP_001341826.1:p.Arg1686Gly | |
| NM_001354898.1:c.4951A>G | NP_001341827.1:p.Arg1651Gly | |
| NM_001354899.1:c.4942A>G | NP_001341828.1:p.Arg1648Gly | |
| NM_001354900.1:c.4903A>G | NP_001341829.1:p.Arg1635Gly | |
| NM_001354901.1:c.4849A>G | NP_001341830.1:p.Arg1617Gly | |
| NM_001354902.1:c.4753A>G | NP_001341831.1:p.Arg1585Gly | |
| NM_001354903.1:c.4723A>G | NP_001341832.1:p.Arg1575Gly | |
| NM_001354904.1:c.4648A>G | NP_001341833.1:p.Arg1550Gly | |
| NM_001354905.1:c.4546A>G | NP_001341834.1:p.Arg1516Gly | |
| NM_001354906.1:c.4177A>G | NP_001341835.1:p.Arg1393Gly | |
| NM_000038.6:c.5026A>G MANE Select | NP_000029.2:p.Arg1676Gly | |
| NM_001127510.3:c.5026A>G | NP_001120982.1:p.Arg1676Gly | |
| NM_001127511.3:c.4972A>G | NP_001120983.2:p.Arg1658Gly | |
| NM_001354895.2:c.5026A>G | NP_001341824.1:p.Arg1676Gly | |
| NM_001354896.2:c.5080A>G | NP_001341825.1:p.Arg1694Gly | |
| NM_001354897.2:c.5056A>G | NP_001341826.1:p.Arg1686Gly | |
| NM_001354898.2:c.4951A>G | NP_001341827.1:p.Arg1651Gly | |
| NM_001354899.2:c.4942A>G | NP_001341828.1:p.Arg1648Gly | |
| NM_001354900.2:c.4903A>G | NP_001341829.1:p.Arg1635Gly | |
| NM_001354901.2:c.4849A>G | NP_001341830.1:p.Arg1617Gly | |
| NM_001354902.2:c.4753A>G | NP_001341831.1:p.Arg1585Gly | |
| NM_001354903.2:c.4723A>G | NP_001341832.1:p.Arg1575Gly | |
| NM_001354904.2:c.4648A>G | NP_001341833.1:p.Arg1550Gly | |
| NM_001354905.2:c.4546A>G | NP_001341834.1:p.Arg1516Gly | |
| NM_001354906.2:c.4177A>G | NP_001341835.1:p.Arg1393Gly |