Linked Data
ClinVar Variation Id:
358942
dbSNP Id:
rs143303575
ExAC:
7:130041748 G / C
gnomAD v2:
7-130041748-G-C
gnomAD v3:
7-130401907-G-C
gnomAD v4:
7-130401907-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.130401907G>C , CM000669.2:g.130401907G>C | GRCh38 |
| NC_000007.13:g.130041748G>C , CM000669.1:g.130041748G>C | GRCh37 |
| NC_000007.12:g.129828984G>C | NCBI36 |
| NG_032164.1:g.44304C>G | |
| NG_032164.2:g.44304C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000223208.10:c.616C>G MANE Select | ENSP00000223208.4:p.Pro206Ala | |
| ENST00000343969.10:c.616C>G | ENSP00000342738.6:p.Pro206Ala | |
| ENST00000471201.6:c.829C>G | ENSP00000417463.2:p.Pro277Ala | |
| ENST00000472739.6:c.511C>G | ENSP00000417593.2:p.Pro171Ala | |
| ENST00000475282.6:c.511C>G | ENSP00000418363.2:p.Pro171Ala | |
| ENST00000477003.6:c.*218C>G | ENSP00000420670.2:n.*218C>G | |
| ENST00000480206.2:c.616C>G | ENSP00000502099.1:p.Pro206Ala | |
| ENST00000484549.6:c.*788C>G | ENSP00000419078.2:n.*788C>G | |
| ENST00000492389.6:c.636C>G | ENSP00000419192.2:n.636C>G | |
| ENST00000541543.6:c.607C>G | ENSP00000445888.2:p.Pro203Ala | |
| ENST00000674539.1:c.422+2657C>G | ENSP00000502834.1:n.422+2657C>G | |
| ENST00000674630.1:c.*162C>G | ENSP00000502521.1:n.*162C>G | |
| ENST00000675138.1:c.661C>G | ENSP00000501597.1:p.Pro221Ala | |
| ENST00000675168.1:c.568C>G | ENSP00000501563.1:p.Pro190Ala | |
| ENST00000675328.1:n.426C>G | ||
| ENST00000675542.1:n.581C>G | ||
| ENST00000675563.1:c.7C>G | ENSP00000502483.1:p.Pro3Ala | |
| ENST00000675596.1:c.616C>G | ENSP00000501735.1:p.Pro206Ala | |
| ENST00000675649.1:c.574+741C>G | ENSP00000502385.1:n.574+741C>G | |
| ENST00000675721.1:c.*559C>G | ENSP00000502026.1:n.*559C>G | |
| ENST00000675803.1:c.577C>G | ENSP00000502477.1:p.Pro193Ala | |
| ENST00000675813.1:c.*520C>G | ENSP00000502785.1:n.*520C>G | |
| ENST00000675935.1:c.607C>G | ENSP00000501731.1:p.Pro203Ala | |
| ENST00000675962.1:c.568C>G | ENSP00000502478.1:p.Pro190Ala | |
| ENST00000676115.1:c.*537C>G | ENSP00000502631.1:n.*537C>G | |
| ENST00000676243.1:c.616C>G | ENSP00000501717.1:p.Pro206Ala | |
| ENST00000676312.1:c.577C>G | ENSP00000502312.1:p.Pro193Ala | |
| ENST00000223208.9:c.616C>G | ENSP00000223208.4:p.Pro206Ala | |
| ENST00000343969.9:c.616C>G | ENSP00000342738.5:p.Pro206Ala | |
| ENST00000480206.1:n.81C>G | ||
| ENST00000484549.5:c.*162C>G | ENSP00000419078.1:n.*162C>G | |
| ENST00000492389.5:c.511C>G | ENSP00000419192.1:p.Pro171Ala | |
| ENST00000541543.5:c.568C>G | ENSP00000445888.1:p.Pro190Ala | |
| NM_001257158.1:c.616C>G | NP_001244087.1:p.Pro206Ala | |
| NM_001257159.1:c.568C>G | NP_001244088.1:p.Pro190Ala | |
| NM_018718.2:c.616C>G | NP_061188.1:p.Pro206Ala | |
| NR_046443.1:n.784C>G | ||
| XM_011516708.1:c.661C>G | XP_011515010.1:p.Pro221Ala | |
| XM_011516709.1:c.511C>G | XP_011515011.1:p.Pro171Ala | |
| XM_011516710.1:c.511C>G | XP_011515012.1:p.Pro171Ala | |
| XM_011516711.1:c.511C>G | XP_011515013.1:p.Pro171Ala | |
| XM_011516712.1:c.661C>G | XP_011515014.1:p.Pro221Ala | |
| XM_011516709.3:c.511C>G | XP_011515011.1:p.Pro171Ala | |
| XM_011516710.3:c.511C>G | XP_011515012.1:p.Pro171Ala | |
| XM_024447004.1:c.577C>G | XP_024302772.1:p.Pro193Ala | |
| NM_018718.3:c.616C>G MANE Select | NP_061188.1:p.Pro206Ala | |
| NM_001257158.2:c.616C>G | NP_001244087.1:p.Pro206Ala | |
| NR_046443.2:n.590C>G | ||
| NM_001257159.2:c.568C>G | NP_001244088.1:p.Pro190Ala |