Linked Data
ClinVar Variation Id:
3228122
ClinVar RCV Id:
RCV004519832
MyVariant Identifiers:
chr17:g.59761179T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61683818T>G , CM000679.2:g.61683818T>G | GRCh38 |
| NC_000017.10:g.59761179T>G , CM000679.1:g.59761179T>G | GRCh37 |
| NC_000017.9:g.57115961T>G | NCBI36 |
| NG_007409.2:g.184742A>C , LRG_300:g.184742A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682073.1:n.1968A>C | ||
| ENST00000682453.1:c.3228A>C | ENSP00000506943.1:p.Ser1076= | |
| ENST00000682477.1:c.*2654A>C | ENSP00000507075.1:n.*2654A>C | |
| ENST00000682589.1:n.9105A>C | ||
| ENST00000682755.1:c.3006A>C | ENSP00000507660.1:p.Ser1002= | |
| ENST00000682989.1:c.*319A>C | ENSP00000507786.1:n.*319A>C | |
| ENST00000683039.1:c.3228A>C | ENSP00000508303.1:p.Ser1076= | |
| ENST00000683235.1:c.*643A>C | ENSP00000507646.1:n.*643A>C | |
| ENST00000683535.1:n.1358A>C | ||
| ENST00000684584.1:c.2391A>C | ENSP00000508044.1:p.Ser797= | |
| ENST00000684626.1:n.1474A>C | ||
| ENST00000684769.1:c.1418A>C | ENSP00000507691.1:n.1418A>C | |
| ENST00000259008.7:c.3228A>C MANE Select | ENSP00000259008.2:p.Ser1076= | |
| ENST00000259008.6:c.3228A>C | ENSP00000259008.2:p.Ser1076= | |
| NM_032043.2:c.3228A>C , LRG_300t1:c.3228A>C | NP_114432.2:p.Ser1076= | |
| XM_011525332.1:c.3288A>C | XP_011523634.1:p.Ser1096= | |
| XM_011525333.1:c.3288A>C | XP_011523635.1:p.Ser1096= | |
| XM_011525334.1:c.3288A>C | XP_011523636.1:p.Ser1096= | |
| XM_011525335.1:c.3228A>C | XP_011523637.1:p.Ser1076= | |
| XM_011525336.1:c.3168A>C | XP_011523638.1:p.Ser1056= | |
| XM_011525337.1:c.3087A>C | XP_011523639.1:p.Ser1029= | |
| XM_011525338.1:c.2805A>C | XP_011523640.1:p.Ser935= | |
| XM_011525332.3:c.3288A>C | XP_011523634.1:p.Ser1096= | |
| XM_011525333.3:c.3288A>C | XP_011523635.1:p.Ser1096= | |
| XM_011525334.2:c.3288A>C | XP_011523636.1:p.Ser1096= | |
| XM_011525335.3:c.3228A>C | XP_011523637.1:p.Ser1076= | |
| XM_011525336.2:c.3168A>C | XP_011523638.1:p.Ser1056= | |
| XM_011525337.2:c.3087A>C | XP_011523639.1:p.Ser1029= | |
| XM_011525338.2:c.2805A>C | XP_011523640.1:p.Ser935= | |
| XM_017025200.1:c.2745A>C | XP_016880689.1:p.Ser915= | |
| XM_017025201.1:c.2745A>C | XP_016880690.1:p.Ser915= | |
| XM_017025202.1:c.1374A>C | XP_016880691.1:p.Ser458= | |
| XM_017025203.1:c.1374A>C | XP_016880692.1:p.Ser458= | |
| NM_032043.3:c.3228A>C MANE Select | NP_114432.2:p.Ser1076= |