MyVariant.info:
GRCh37
chr9:g.138656945G>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.135765099G>C , CM000671.2:g.135765099G>C | GRCh38 |
| NC_000009.11:g.138656945G>C , CM000671.1:g.138656945G>C | GRCh37 |
| NC_000009.10:g.137796766G>C | NCBI36 |
| NG_033070.1:g.67915G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371757.7:c.1104G>C MANE Select | ENSP00000360822.2:p.Ala368= | |
| ENST00000674572.1:c.945G>C | ENSP00000501742.1:p.Ala315= | |
| ENST00000675090.1:c.852G>C | ENSP00000501833.1:p.Ala284= | |
| ENST00000675399.1:c.852G>C | ENSP00000501932.1:p.Ala284= | |
| ENST00000676421.1:c.861G>C | ENSP00000502322.1:p.Ala287= | |
| ENST00000263604.5:c.1005G>C | ENSP00000263604.4:p.Ala335= | |
| ENST00000371757.6:c.1104G>C | ENSP00000360822.2:p.Ala368= | |
| ENST00000460750.5:c.*714G>C | ENSP00000418777.1:n.*714G>C | |
| ENST00000486577.6:c.987G>C | ENSP00000417578.3:p.Ala329= | |
| ENST00000487664.5:c.1104G>C | ENSP00000417851.2:p.Ala368= | |
| ENST00000488444.6:c.1047G>C | ENSP00000419007.3:p.Ala349= | |
| ENST00000490355.6:c.1047G>C | ENSP00000418003.3:p.Ala349= | |
| ENST00000490363.3:n.923G>C | ||
| ENST00000491806.6:c.1047G>C | ENSP00000419086.3:p.Ala349= | |
| ENST00000628528.2:c.969G>C | ENSP00000486374.1:p.Ala323= | |
| ENST00000630792.2:c.945G>C | ENSP00000486486.1:p.Ala315= | |
| ENST00000631073.2:c.1047G>C | ENSP00000486130.1:p.Ala349= | |
| NM_001272003.1:c.969G>C | NP_001258932.1:p.Ala323= | |
| NM_020822.2:c.1104G>C | NP_065873.2:p.Ala368= | |
| XM_011518877.1:c.1239G>C | XP_011517179.1:p.Ala413= | |
| XM_011518878.1:c.1248G>C | XP_011517180.1:p.Ala416= | |
| XM_011518879.1:c.1239G>C | XP_011517181.1:p.Ala413= | |
| XM_011518880.1:c.1005G>C | XP_011517182.1:p.Ala335= | |
| XM_011518881.1:c.594G>C | XP_011517183.1:p.Ala198= | |
| XM_011518877.3:c.1239G>C | XP_011517179.1:p.Ala413= | |
| XM_011518878.3:c.1248G>C | XP_011517180.1:p.Ala416= | |
| XM_011518879.3:c.1239G>C | XP_011517181.1:p.Ala413= | |
| XM_011518881.3:c.594G>C | XP_011517183.1:p.Ala198= | |
| XM_017014931.1:c.1038G>C | XP_016870420.1:p.Ala346= | |
| XM_017014932.1:c.861G>C | XP_016870421.1:p.Ala287= | |
| XM_017014933.1:c.594G>C | XP_016870422.1:p.Ala198= | |
| XM_024447617.1:c.594G>C | XP_024303385.1:p.Ala198= | |
| XM_024447618.1:c.594G>C | XP_024303386.1:p.Ala198= | |
| NM_020822.3:c.1104G>C MANE Select | NP_065873.2:p.Ala368= | |
| NM_001272003.2:c.969G>C | NP_001258932.1:p.Ala323= |