MyVariant.info:
GRCh37
chr16:g.68862157C>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68828254C>A , CM000678.2:g.68828254C>A | GRCh38 |
| NC_000016.9:g.68862157C>A , CM000678.1:g.68862157C>A | GRCh37 |
| NC_000016.8:g.67419658C>A | NCBI36 |
| NG_008021.1:g.95963C>A , LRG_301:g.95963C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.2245C>A MANE Select | ENSP00000261769.4:p.Arg749= | |
| ENST00000261769.9:c.2245C>A | ENSP00000261769.4:p.Arg749= | |
| ENST00000422392.6:c.2062C>A | ENSP00000414946.2:p.Arg688= | |
| ENST00000562118.1:n.463C>A | ||
| ENST00000562836.5:n.2316C>A | ||
| ENST00000566510.5:c.*911C>A | ENSP00000458139.1:n.*911C>A | |
| ENST00000566612.5:c.*485C>A | ENSP00000454782.1:n.*485C>A | |
| ENST00000611625.4:c.2308C>A | ENSP00000481063.1:p.Arg770= | |
| ENST00000612417.4:c.1853+1700C>A | ENSP00000478360.1:n.1853+1700C>A | |
| ENST00000621016.4:c.1866-5949C>A | ENSP00000480664.1:n.1866-5949C>A | |
| NM_004360.3:c.2245C>A , LRG_301t1:c.2245C>A | NP_004351.1:p.Arg749= | |
| XM_011523488.1:c.1510C>A | XP_011521790.1:p.Arg504= | |
| XM_011523489.1:c.1510C>A | XP_011521791.1:p.Arg504= | |
| NM_001317184.1:c.2062C>A | NP_001304113.1:p.Arg688= | |
| NM_001317185.1:c.697C>A | NP_001304114.1:p.Arg233= | |
| NM_001317186.1:c.280C>A | NP_001304115.1:p.Arg94= | |
| NM_004360.4:c.2245C>A | NP_004351.1:p.Arg749= | |
| NM_004360.5:c.2245C>A MANE Select | NP_004351.1:p.Arg749= | |
| NM_001317184.2:c.2062C>A | NP_001304113.1:p.Arg688= | |
| NM_001317185.2:c.697C>A | NP_001304114.1:p.Arg233= | |
| NM_001317186.2:c.280C>A | NP_001304115.1:p.Arg94= |