Linked Data
ClinVar Variation Id:
228601
dbSNP Id:
rs138838276
ExAC:
16:84203933 C / G
gnomAD v2:
16-84203933-C-G
gnomAD v3:
16-84170327-C-G
gnomAD v4:
16-84170327-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.84170327C>G , CM000678.2:g.84170327C>G | GRCh38 |
| NC_000016.9:g.84203933C>G , CM000678.1:g.84203933C>G | GRCh37 |
| NC_000016.8:g.82761434C>G | NCBI36 |
| NG_021174.1:g.30069C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378553.10:c.1499C>G MANE Select | ENSP00000367815.5:p.Pro500Arg | |
| ENST00000378553.9:c.1499C>G | ENSP00000367815.5:p.Pro500Arg | |
| ENST00000563093.5:c.*54C>G | ENSP00000457373.1:n.*54C>G | |
| ENST00000563818.5:n.1176C>G | ||
| ENST00000570298.5:n.1653C>G | ||
| NM_178452.4:c.1499C>G | NP_848547.4:p.Pro500Arg | |
| XM_006721129.1:c.1499C>G | XP_006721192.1:p.Pro500Arg | |
| XM_011522850.1:c.1547C>G | XP_011521152.1:p.Pro516Arg | |
| XM_011522851.1:c.1547C>G | XP_011521153.1:p.Pro516Arg | |
| XM_011522852.1:c.1499C>G | XP_011521154.1:p.Pro500Arg | |
| XM_011522853.1:c.1547C>G | XP_011521155.1:p.Pro516Arg | |
| XM_011522854.1:c.1547C>G | XP_011521156.1:p.Pro516Arg | |
| XM_011522855.1:c.1547C>G | XP_011521157.1:p.Pro516Arg | |
| XM_011522856.1:c.1286C>G | XP_011521158.1:p.Pro429Arg | |
| XM_011522857.1:c.1547C>G | XP_011521159.1:p.Pro516Arg | |
| XM_011522858.1:c.1547C>G | XP_011521160.1:p.Pro516Arg | |
| XM_011522859.1:c.791C>G | XP_011521161.1:p.Pro264Arg | |
| XM_011522860.1:c.791C>G | XP_011521162.1:p.Pro264Arg | |
| NM_001318756.1:c.791C>G | NP_001305685.1:p.Pro264Arg | |
| NM_178452.5:c.1499C>G | NP_848547.4:p.Pro500Arg | |
| XM_006721129.3:c.1499C>G | XP_006721192.1:p.Pro500Arg | |
| XM_011522853.3:c.1547C>G | XP_011521155.1:p.Pro516Arg | |
| XM_011522854.3:c.1547C>G | XP_011521156.1:p.Pro516Arg | |
| XM_011522855.3:c.1547C>G | XP_011521157.1:p.Pro516Arg | |
| XM_011522857.3:c.1547C>G | XP_011521159.1:p.Pro516Arg | |
| XM_011522858.3:c.1547C>G | XP_011521160.1:p.Pro516Arg | |
| XM_017022918.2:c.1499C>G | XP_016878407.1:p.Pro500Arg | |
| XM_017022919.1:c.1286C>G | XP_016878408.1:p.Pro429Arg | |
| XM_017022920.2:c.791C>G | XP_016878409.1:p.Pro264Arg | |
| XM_017022921.2:c.743C>G | XP_016878410.1:p.Pro248Arg | |
| XM_017022922.2:c.743C>G | XP_016878411.1:p.Pro248Arg | |
| XR_001751829.2:n.1721C>G | ||
| XR_001751830.2:n.1721C>G | ||
| XR_001751831.2:n.1673C>G | ||
| XR_001751832.1:n.1982C>G | ||
| NM_178452.6:c.1499C>G MANE Select | NP_848547.4:p.Pro500Arg |