Linked Data
dbSNP Id:
rs777023979
ExAC:
7:107340538 C / G
gnomAD v2:
7-107340538-C-G
gnomAD v4:
7-107700093-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107700093C>G , CM000669.2:g.107700093C>G | GRCh38 |
| NC_000007.13:g.107340538C>G , CM000669.1:g.107340538C>G | GRCh37 |
| NC_000007.12:g.107127774C>G | NCBI36 |
| NG_008489.1:g.44459C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.1625C>G MANE Select | ENSP00000494017.1:p.Pro542Arg | |
| ENST00000644846.1:c.336C>G | ||
| ENST00000265715.7:c.1625C>G | ENSP00000265715.3:p.Pro542Arg | |
| ENST00000477350.5:n.472C>G | ||
| ENST00000480841.5:n.474C>G | ||
| ENST00000492030.2:n.8C>G | ||
| NM_000441.1:c.1625C>G | NP_000432.1:p.Pro542Arg | |
| XM_005250425.1:c.1625C>G | XP_005250482.1:p.Pro542Arg | |
| XM_005250425.2:c.1625C>G | XP_005250482.1:p.Pro542Arg | |
| XM_017012318.1:c.1547C>G | XP_016867807.1:p.Pro516Arg | |
| NM_000441.2:c.1625C>G MANE Select | NP_000432.1:p.Pro542Arg |