Linked Data
ClinVar Variation Id:
383321
dbSNP Id:
rs903555499
gnomAD v3:
20-63406932-G-A
gnomAD v4:
20-63406932-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.63406932G>A , CM000682.2:g.63406932G>A | GRCh38 |
| NC_000020.10:g.62038285G>A , CM000682.1:g.62038285G>A | GRCh37 |
| NC_000020.9:g.61508729G>A | NCBI36 |
| NG_009004.1:g.70709C>T | |
| NG_009004.2:g.70709C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706989.1:c.2385C>T | ENSP00000516702.1:p.Pro795= | |
| ENST00000359125.7:c.2331C>T MANE Select | ENSP00000352035.2:p.Pro777= | |
| ENST00000637193.1:c.1728C>T | ENSP00000490734.1:p.Pro576= | |
| ENST00000344462.8:c.2238C>T | ENSP00000339611.4:p.Pro746= | |
| ENST00000357249.6:c.1899C>T | ENSP00000349789.3:p.Pro633= | |
| ENST00000359125.6:c.2331C>T | ENSP00000352035.2:p.Pro777= | |
| ENST00000360480.7:c.2247C>T | ENSP00000353668.3:p.Pro749= | |
| ENST00000370224.5:c.2241+114C>T | ENSP00000359244.2:n.2241+114C>T | |
| ENST00000625514.2:c.2205+114C>T | ENSP00000486040.1:n.2205+114C>T | |
| ENST00000626839.2:c.2277C>T | ENSP00000486706.1:p.Pro759= | |
| ENST00000629241.2:c.2133+114C>T | ENSP00000487142.1:n.2133+114C>T | |
| ENST00000629676.2:c.1680-6089C>T | ENSP00000486194.1:n.1680-6089C>T | |
| NM_004518.4:c.2247C>T | NP_004509.2:p.Pro749= | |
| NM_172106.1:c.2277C>T | NP_742104.1:p.Pro759= | |
| NM_172107.2:c.2331C>T | NP_742105.1:p.Pro777= | |
| NM_172108.3:c.2238C>T | NP_742106.1:p.Pro746= | |
| XM_006723787.1:c.2373C>T | XP_006723850.1:p.Pro791= | |
| XM_011528807.1:c.2439C>T | XP_011527109.1:p.Pro813= | |
| XM_011528808.1:c.2436C>T | XP_011527110.1:p.Pro812= | |
| XM_011528809.1:c.2409C>T | XP_011527111.1:p.Pro803= | |
| XM_011528810.1:c.2385C>T | XP_011527112.1:p.Pro795= | |
| XM_011528811.1:c.2355C>T | XP_011527113.1:p.Pro785= | |
| XM_011528812.1:c.2328C>T | XP_011527114.1:p.Pro776= | |
| XM_011528813.1:c.2313C>T | XP_011527115.1:p.Pro771= | |
| XM_011528814.1:c.1920C>T | XP_011527116.1:p.Pro640= | |
| NM_004518.5:c.2247C>T | NP_004509.2:p.Pro749= | |
| NM_172106.2:c.2277C>T | NP_742104.1:p.Pro759= | |
| NM_172107.3:c.2331C>T | NP_742105.1:p.Pro777= | |
| NM_172108.4:c.2238C>T | NP_742106.1:p.Pro746= | |
| XM_011528810.2:c.2385C>T | XP_011527112.1:p.Pro795= | |
| XM_011528811.2:c.2355C>T | XP_011527113.1:p.Pro785= | |
| XM_017027841.2:c.2382C>T | XP_016883330.1:p.Pro794= | |
| XM_017027842.2:c.2319C>T | XP_016883331.1:p.Pro773= | |
| XM_017027843.1:c.2316C>T | XP_016883332.1:p.Pro772= | |
| XM_017027844.2:c.2274C>T | XP_016883333.1:p.Pro758= | |
| XM_017027845.1:c.1347C>T | XP_016883334.1:p.Pro449= | |
| NM_004518.6:c.2247C>T | NP_004509.2:p.Pro749= | |
| NM_172106.3:c.2277C>T | NP_742104.1:p.Pro759= | |
| NM_172107.4:c.2331C>T MANE Select | NP_742105.1:p.Pro777= | |
| NM_172108.5:c.2238C>T | NP_742106.1:p.Pro746= | |
| NM_001382235.1:c.2385C>T | NP_001369164.1:p.Pro795= |