Linked Data
ClinVar Variation Id:
302205
dbSNP Id:
rs150038447
ExAC:
11:108014748 A / G
gnomAD v2:
11-108014748-A-G
gnomAD v3:
11-108144021-A-G
gnomAD v4:
11-108144021-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108144021A>G , CM000673.2:g.108144021A>G | GRCh38 |
| NC_000011.9:g.108014748A>G , CM000673.1:g.108014748A>G | GRCh37 |
| NC_000011.8:g.107519958A>G | NCBI36 |
| NG_009888.1:g.27491A>G | |
| NG_009888.2:g.32317A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265838.9:c.979A>G MANE Select | ENSP00000265838.4:p.Ile327Val | |
| ENST00000671707.1:n.1074A>G | ||
| ENST00000672031.1:c.940+1471A>G | ENSP00000500463.1:n.940+1471A>G | |
| ENST00000672284.1:c.709A>G | ENSP00000500444.1:p.Ile237Val | |
| ENST00000672354.1:c.979A>G | ENSP00000500490.1:p.Ile327Val | |
| ENST00000672367.1:c.616A>G | ENSP00000500209.1:p.Ile206Val | |
| ENST00000672580.1:c.*234A>G | ENSP00000500366.1:n.*234A>G | |
| ENST00000672907.1:c.664A>G | ENSP00000500928.1:p.Ile222Val | |
| ENST00000673000.1:n.1067A>G | ||
| ENST00000673531.1:c.709A>G | ENSP00000500163.1:p.Ile237Val | |
| ENST00000265838.8:c.979A>G | ENSP00000265838.4:p.Ile327Val | |
| ENST00000532792.5:n.474A>G | ||
| ENST00000533610.1:n.440A>G | ||
| NM_000019.3:c.979A>G | NP_000010.1:p.Ile327Val | |
| XM_006718834.2:c.709A>G | XP_006718897.1:p.Ile237Val | |
| XM_006718835.2:c.709A>G | XP_006718898.1:p.Ile237Val | |
| XM_006718835.3:c.709A>G | XP_006718898.1:p.Ile237Val | |
| XM_017017681.1:c.709A>G | XP_016873170.1:p.Ile237Val | |
| XM_017017682.2:c.601A>G | XP_016873171.1:p.Ile201Val | |
| XM_017017683.2:c.601A>G | XP_016873172.1:p.Ile201Val | |
| XM_024448511.1:c.709A>G | XP_024304279.1:p.Ile237Val | |
| XM_024448512.1:c.709A>G | XP_024304280.1:p.Ile237Val | |
| XM_024448513.1:c.709A>G | XP_024304281.1:p.Ile237Val | |
| XM_024448514.1:c.709A>G | XP_024304282.1:p.Ile237Val | |
| XM_024448515.1:c.709A>G | XP_024304283.1:p.Ile237Val | |
| NM_000019.4:c.979A>G MANE Select | NP_000010.1:p.Ile327Val | |
| NM_001386677.1:c.979A>G | NP_001373606.1:p.Ile327Val | |
| NM_001386678.1:c.664A>G | NP_001373607.1:p.Ile222Val | |
| NM_001386679.1:c.682A>G | NP_001373608.1:p.Ile228Val | |
| NM_001386681.1:c.709A>G | NP_001373610.1:p.Ile237Val | |
| NM_001386682.1:c.709A>G | NP_001373611.1:p.Ile237Val | |
| NM_001386685.1:c.709A>G | NP_001373614.1:p.Ile237Val | |
| NM_001386686.1:c.709A>G | NP_001373615.1:p.Ile237Val | |
| NM_001386687.1:c.709A>G | NP_001373616.1:p.Ile237Val | |
| NM_001386688.1:c.709A>G | NP_001373617.1:p.Ile237Val | |
| NM_001386689.1:c.709A>G | NP_001373618.1:p.Ile237Val | |
| NM_001386690.1:c.709A>G | NP_001373619.1:p.Ile237Val | |
| NM_001386691.1:c.709A>G | NP_001373620.1:p.Ile237Val | |
| NR_170162.1:n.980+1471A>G | ||
| NR_170163.1:n.1012A>G |