Linked Data
MyVariant Identifiers:
chr19:g.15651436C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15540625C>A , CM000681.2:g.15540625C>A | GRCh38 |
| NC_000019.9:g.15651436C>A , CM000681.1:g.15651436C>A | GRCh37 |
| NC_000019.8:g.15512436C>A | NCBI36 |
| NG_007987.1:g.37101C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269703.8:c.847C>A MANE Select | ENSP00000269703.1:p.Arg283= | |
| ENST00000269703.7:c.847C>A | ENSP00000269703.1:p.Arg283= | |
| ENST00000601005.2:c.847C>A | ENSP00000469866.1:p.Arg283= | |
| NM_173483.3:c.847C>A | NP_775754.2:p.Arg283= | |
| XM_011527692.1:c.847C>A | XP_011525994.1:p.Arg283= | |
| XM_011527693.1:c.847C>A | XP_011525995.1:p.Arg283= | |
| XM_011527692.2:c.847C>A | XP_011525994.1:p.Arg283= | |
| XM_011527693.2:c.847C>A | XP_011525995.1:p.Arg283= | |
| NM_173483.4:c.847C>A MANE Select | NP_775754.2:p.Arg283= |