MyVariant.info:
GRCh37
chr6:g.157469898C>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.157148764C>A , CM000668.2:g.157148764C>A | GRCh38 |
| NC_000006.11:g.157469898C>A , CM000668.1:g.157469898C>A | GRCh37 |
| NC_000006.10:g.157511590C>A | NCBI36 |
| NG_032093.1:g.375835C>A | |
| NG_032093.2:g.375835C>A | |
| NG_066624.1:g.377739C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000350026.11:c.2902C>A | ENSP00000055163.8:p.Arg968= | |
| ENST00000414678.8:c.2812C>A | ENSP00000412835.3:p.Arg938= | |
| ENST00000637015.2:c.2902C>A | ENSP00000489729.2:p.Arg968= | |
| ENST00000319584.11:c.916C>A | ENSP00000313006.7:p.Arg306= | |
| ENST00000346085.10:c.2941C>A | ENSP00000344546.5:p.Arg981= | |
| ENST00000350026.10:c.2653C>A | ENSP00000055163.7:p.Arg885= | |
| ENST00000414678.7:c.1060C>A | ENSP00000412835.2:p.Arg354= | |
| ENST00000452544.2:n.803C>A | ||
| ENST00000635849.1:c.223C>A | ENSP00000490948.1:p.Arg75= | |
| ENST00000636426.1:n.36C>A | ||
| ENST00000636930.2:c.2902C>A MANE Select | ENSP00000490491.2:p.Arg968= | |
| ENST00000637015.1:c.141C>A | ||
| ENST00000637810.1:c.403C>A | ENSP00000489636.1:p.Arg135= | |
| ENST00000637904.1:c.403C>A | ENSP00000490550.1:p.Arg135= | |
| ENST00000647938.1:c.2692C>A | ENSP00000498155.1:p.Arg898= | |
| ENST00000674190.1:n.1651C>A | ||
| ENST00000319584.10:c.919C>A | ENSP00000313006.6:p.Arg307= | |
| ENST00000346085.9:c.2692C>A | ENSP00000344546.4:p.Arg898= | |
| ENST00000350026.9:c.2653C>A | ENSP00000055163.7:p.Arg885= | |
| ENST00000414678.6:c.1060C>A | ENSP00000412835.2:p.Arg354= | |
| ENST00000452544.1:n.749C>A | ||
| NM_017519.2:c.2653C>A | NP_059989.2:p.Arg885= | |
| NM_020732.3:c.2692C>A | NP_065783.3:p.Arg898= | |
| XM_005267069.3:c.2653C>A | XP_005267126.2:p.Arg885= | |
| XM_011535984.1:c.1603C>A | XP_011534286.1:p.Arg535= | |
| XM_011535985.1:c.1423C>A | XP_011534287.1:p.Arg475= | |
| XM_011535986.1:c.1183C>A | XP_011534288.1:p.Arg395= | |
| XM_011535987.1:c.802C>A | XP_011534289.1:p.Arg268= | |
| XM_011535988.1:c.-20+15557C>A | XP_011534290.1:n.-20+15557C>A | |
| NM_001346813.1:c.2653C>A | NP_001333742.1:p.Arg885= | |
| NM_001363725.1:c.403C>A | NP_001350654.1:p.Arg135= | |
| XM_011535984.2:c.2734C>A | XP_011534286.2:p.Arg912= | |
| XM_011535988.3:c.-20+15557C>A | XP_011534290.1:n.-20+15557C>A | |
| XM_017011103.2:c.2734C>A | XP_016866592.1:p.Arg912= | |
| XM_017011104.1:c.2734C>A | XP_016866593.1:p.Arg912= | |
| XM_017011105.2:c.2734C>A | XP_016866594.1:p.Arg912= | |
| XM_017011106.2:c.2734C>A | XP_016866595.1:p.Arg912= | |
| XM_017011107.2:c.2554C>A | XP_016866596.1:p.Arg852= | |
| XR_002956289.1:n.2817C>A | ||
| NM_001363725.2:c.403C>A | NP_001350654.1:p.Arg135= | |
| NM_001371656.1:c.2941C>A | NP_001358585.1:p.Arg981= | |
| NM_001374820.1:c.2941C>A | NP_001361749.1:p.Arg981= | |
| NM_001374828.1:c.2902C>A MANE Select | NP_001361757.1:p.Arg968= | |
| NM_017519.3:c.2902C>A | NP_059989.3:p.Arg968= |