Linked Data
dbSNP Id:
rs1235936772
gnomAD v2:
6-20661049-C-G
gnomAD v3:
6-20660818-C-G
gnomAD v4:
6-20660818-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.20660818C>G , CM000668.2:g.20660818C>G | GRCh38 |
| NC_000006.11:g.20661049C>G , CM000668.1:g.20661049C>G | GRCh37 |
| NC_000006.10:g.20769028C>G | NCBI36 |
| NG_021195.1:g.131362C>G | |
| NG_021195.2:g.131362C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000274695.8:c.371+11441C>G MANE Select | ENSP00000274695.4:n.371+11441C>G | |
| ENST00000378610.1:c.371+11441C>G | ENSP00000367873.1:n.371+11441C>G | |
| NM_017774.3:c.371+11441C>G MANE Select | NP_060244.2:n.371+11441C>G | |
| XM_006715128.2:c.371+11441C>G | XP_006715191.1:n.371+11441C>G | |
| XM_011514718.1:c.371+11441C>G | XP_011513020.1:n.371+11441C>G | |
| XM_011514719.1:c.371+11441C>G | XP_011513021.1:n.371+11441C>G | |
| XR_926265.1:n.538+11441C>G | ||
| XR_926266.1:n.651+11441C>G | ||
| XR_926267.1:n.538+11441C>G | ||
| XM_011514719.2:c.371+11441C>G | XP_011513021.1:n.371+11441C>G | |
| XM_017010986.1:c.371+11441C>G | XP_016866475.1:n.371+11441C>G | |
| XM_017010987.1:c.-384+11441C>G | XP_016866476.1:n.-384+11441C>G | |
| XM_024446481.1:c.371+11441C>G | XP_024302249.1:n.371+11441C>G | |
| XR_001743495.2:n.543+11441C>G | ||
| XR_001743496.2:n.938+11441C>G | ||
| XR_001743500.1:n.538+11441C>G | ||
| XR_001743501.1:n.538+11441C>G | ||
| XR_926265.2:n.538+11441C>G | ||
| XR_926266.2:n.651+11441C>G | ||
| XR_926267.2:n.538+11441C>G |