Linked Data
gnomAD v3:
3-122285041-A-G
gnomAD v4:
3-122285041-A-G
MyVariant Identifiers:
chr3:g.122003888A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.122285041A>G , CM000665.2:g.122285041A>G | GRCh38 |
| NC_000003.11:g.122003888A>G , CM000665.1:g.122003888A>G | GRCh37 |
| NC_000003.10:g.123486578A>G | NCBI36 |
| NG_009058.1:g.106359A>G | |
| NG_009058.2:g.106374A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000490131.7:c.2856A>G | ENSP00000418685.2:p.Glu952= | |
| ENST00000498619.4:c.3117A>G | ENSP00000420194.1:p.Glu1039= | |
| ENST00000638421.1:c.3087A>G | ENSP00000492190.1:p.Glu1029= | |
| ENST00000639785.2:c.3087A>G MANE Select | ENSP00000491584.2:p.Glu1029= | |
| ENST00000490131.5:c.3087A>G | ENSP00000418685.1:p.Glu1029= | |
| ENST00000498619.2:c.3117A>G | ENSP00000420194.1:p.Glu1039= | |
| NM_000388.3:c.3087A>G | NP_000379.2:p.Glu1029= | |
| NM_001178065.1:c.3117A>G | NP_001171536.1:p.Glu1039= | |
| XM_005247836.2:c.3087A>G | XP_005247893.1:p.Glu1029= | |
| XM_005247837.2:c.2604A>G | XP_005247894.1:p.Glu868= | |
| XM_006713789.2:c.3087A>G | XP_006713852.1:p.Glu1029= | |
| XM_011513237.1:c.3087A>G | XP_011511539.1:p.Glu1029= | |
| XM_011513238.1:c.3087A>G | XP_011511540.1:p.Glu1029= | |
| XM_011513239.1:c.2499A>G | XP_011511541.1:p.Glu833= | |
| XM_006713789.3:c.3087A>G | XP_006713852.1:p.Glu1029= | |
| XM_017007324.1:c.3087A>G | XP_016862813.1:p.Glu1029= | |
| XM_017007325.1:c.3087A>G | XP_016862814.1:p.Glu1029= | |
| NM_000388.4:c.3087A>G MANE Select | NP_000379.3:p.Glu1029= | |
| NM_001178065.2:c.3117A>G | NP_001171536.2:p.Glu1039= |