MyVariant.info:
GRCh37
chr6:g.157502271C>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.157181137C>A , CM000668.2:g.157181137C>A | GRCh38 |
| NC_000006.11:g.157502271C>A , CM000668.1:g.157502271C>A | GRCh37 |
| NC_000006.10:g.157543963C>A | NCBI36 |
| NG_032093.1:g.408208C>A | |
| NG_032093.2:g.408208C>A | |
| NG_066624.1:g.410112C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000350026.11:c.3514C>A | ENSP00000055163.8:p.Arg1172= | |
| ENST00000414678.8:c.3583C>A | ENSP00000412835.3:p.Arg1195= | |
| ENST00000637015.2:c.3802C>A | ENSP00000489729.2:p.Arg1268= | |
| ENST00000319584.11:c.1687C>A | ENSP00000313006.7:p.Arg563= | |
| ENST00000346085.10:c.3553C>A | ENSP00000344546.5:p.Arg1185= | |
| ENST00000350026.10:c.3265C>A | ENSP00000055163.7:p.Arg1089= | |
| ENST00000414678.7:c.1831C>A | ENSP00000412835.2:p.Arg611= | |
| ENST00000635849.1:c.994C>A | ENSP00000490948.1:p.Arg332= | |
| ENST00000635957.1:c.628C>A | ENSP00000490385.1:p.Arg210= | |
| ENST00000636930.2:c.3673C>A MANE Select | ENSP00000490491.2:p.Arg1225= | |
| ENST00000636940.1:n.1670C>A | ||
| ENST00000637015.1:c.1041C>A | ||
| ENST00000637568.1:c.955C>A | ||
| ENST00000637741.1:n.339C>A | ||
| ENST00000637810.1:c.1015C>A | ENSP00000489636.1:p.Arg339= | |
| ENST00000637904.1:c.1174C>A | ENSP00000490550.1:p.Arg392= | |
| ENST00000647938.1:c.3304C>A | ENSP00000498155.1:p.Arg1102= | |
| ENST00000319584.10:c.1690C>A | ENSP00000313006.6:p.Arg564= | |
| ENST00000346085.9:c.3304C>A | ENSP00000344546.4:p.Arg1102= | |
| ENST00000350026.9:c.3265C>A | ENSP00000055163.7:p.Arg1089= | |
| ENST00000400790.3:c.466C>A | ENSP00000383596.3:p.Arg156= | |
| ENST00000414678.6:c.1831C>A | ENSP00000412835.2:p.Arg611= | |
| ENST00000478761.3:c.875C>A | ||
| NM_017519.2:c.3265C>A | NP_059989.2:p.Arg1089= | |
| NM_020732.3:c.3304C>A | NP_065783.3:p.Arg1102= | |
| XM_005267069.3:c.3424C>A | XP_005267126.2:p.Arg1142= | |
| XM_011535984.1:c.2503C>A | XP_011534286.1:p.Arg835= | |
| XM_011535985.1:c.2323C>A | XP_011534287.1:p.Arg775= | |
| XM_011535986.1:c.2083C>A | XP_011534288.1:p.Arg695= | |
| XM_011535987.1:c.1702C>A | XP_011534289.1:p.Arg568= | |
| XM_011535988.1:c.565C>A | XP_011534290.1:p.Arg189= | |
| NM_001346813.1:c.3424C>A | NP_001333742.1:p.Arg1142= | |
| NM_001363725.1:c.1174C>A | NP_001350654.1:p.Arg392= | |
| XM_011535984.2:c.3634C>A | XP_011534286.2:p.Arg1212= | |
| XM_011535988.3:c.565C>A | XP_011534290.1:p.Arg189= | |
| XM_017011103.2:c.3535C>A | XP_016866592.1:p.Arg1179= | |
| XM_017011104.1:c.3505C>A | XP_016866593.1:p.Arg1169= | |
| XM_017011105.2:c.3475C>A | XP_016866594.1:p.Arg1159= | |
| XM_017011106.2:c.3346C>A | XP_016866595.1:p.Arg1116= | |
| XM_017011107.2:c.3325C>A | XP_016866596.1:p.Arg1109= | |
| XR_002956289.1:n.3717C>A | ||
| NM_001363725.2:c.1174C>A | NP_001350654.1:p.Arg392= | |
| NM_001371656.1:c.3553C>A | NP_001358585.1:p.Arg1185= | |
| NM_001374820.1:c.3553C>A | NP_001361749.1:p.Arg1185= | |
| NM_001374828.1:c.3673C>A MANE Select | NP_001361757.1:p.Arg1225= | |
| NM_017519.3:c.3514C>A | NP_059989.3:p.Arg1172= |