Linked Data
ClinVar Variation Id:
289316
dbSNP Id:
rs182941675
ExAC:
11:61724329 G / A
gnomAD v2:
11-61724329-G-A
gnomAD v3:
11-61956857-G-A
gnomAD v4:
11-61956857-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61956857G>A , CM000673.2:g.61956857G>A | GRCh38 |
| NC_000011.9:g.61724329G>A , CM000673.1:g.61724329G>A | GRCh37 |
| NC_000011.8:g.61480905G>A | NCBI36 |
| NG_009033.1:g.11974G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378043.9:c.495G>A MANE Select | ENSP00000367282.4:p.Pro165= | |
| ENST00000378043.8:c.495G>A | ENSP00000367282.4:p.Pro165= | |
| ENST00000449131.6:c.315G>A | ENSP00000399709.2:p.Pro105= | |
| ENST00000524877.5:n.927G>A | ||
| ENST00000524926.5:c.495G>A | ENSP00000432681.1:p.Pro165= | |
| ENST00000526988.1:c.177G>A | ENSP00000433195.1:p.Pro59= | |
| ENST00000529265.5:n.418G>A | ||
| ENST00000533521.5:n.1119G>A | ||
| ENST00000534553.5:c.163+906G>A | ENSP00000431189.1:n.163+906G>A | |
| NM_001139443.1:c.315G>A | NP_001132915.1:p.Pro105= | |
| NM_001300786.1:c.315G>A | NP_001287715.1:p.Pro105= | |
| NM_001300787.1:c.315G>A | NP_001287716.1:p.Pro105= | |
| NM_004183.3:c.495G>A | NP_004174.1:p.Pro165= | |
| XM_005274210.2:c.495G>A | XP_005274267.1:p.Pro165= | |
| XM_005274215.2:c.177G>A | XP_005274272.1:p.Pro59= | |
| XM_005274216.2:c.315G>A | XP_005274273.1:p.Pro105= | |
| XM_005274218.3:c.177G>A | XP_005274275.1:p.Pro59= | |
| XM_005274219.2:c.495G>A | XP_005274276.1:p.Pro165= | |
| XM_005274221.2:c.495G>A | XP_005274278.1:p.Pro165= | |
| XM_011545229.1:c.495G>A | XP_011543531.1:p.Pro165= | |
| XM_011545230.1:c.402G>A | XP_011543532.1:p.Pro134= | |
| XM_011545231.1:c.177G>A | XP_011543533.1:p.Pro59= | |
| XM_011545232.1:c.495G>A | XP_011543534.1:p.Pro165= | |
| NM_001363591.1:c.177G>A | NP_001350520.1:p.Pro59= | |
| NM_001363592.1:c.495G>A | NP_001350521.1:p.Pro165= | |
| NM_001363593.1:c.-681G>A | NP_001350522.1:n.-681G>A | |
| NR_134580.1:n.1075G>A | ||
| XM_005274210.4:c.495G>A | XP_005274267.1:p.Pro165= | |
| XM_005274215.4:c.177G>A | XP_005274272.1:p.Pro59= | |
| XM_005274216.4:c.315G>A | XP_005274273.1:p.Pro105= | |
| XM_005274219.4:c.495G>A | XP_005274276.1:p.Pro165= | |
| XM_005274221.4:c.495G>A | XP_005274278.1:p.Pro165= | |
| XM_011545229.3:c.495G>A | XP_011543531.1:p.Pro165= | |
| XM_011545230.3:c.402G>A | XP_011543532.1:p.Pro134= | |
| XM_017018230.2:c.177G>A | XP_016873719.1:p.Pro59= | |
| XR_001747952.2:n.993G>A | ||
| XR_001747953.2:n.1185G>A | ||
| XR_001747954.2:n.1185G>A | ||
| XR_002957249.1:n.881C>T | ||
| NM_004183.4:c.495G>A MANE Select | NP_004174.1:p.Pro165= | |
| NM_001139443.2:c.315G>A | NP_001132915.1:p.Pro105= | |
| NM_001300786.2:c.315G>A | NP_001287715.1:p.Pro105= | |
| NM_001300787.2:c.315G>A | NP_001287716.1:p.Pro105= | |
| NM_001363591.2:c.177G>A | NP_001350520.1:p.Pro59= | |
| NM_001363593.2:c.-681G>A | NP_001350522.1:n.-681G>A | |
| NR_134580.2:n.608G>A |