Linked Data
MyVariant Identifiers:
chr1:g.67519565C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67053882C>A , CM000663.2:g.67053882C>A | GRCh38 |
| NC_000001.10:g.67519565C>A , CM000663.1:g.67519565C>A | GRCh37 |
| NC_000001.9:g.67292153C>A | NCBI36 |
| NG_012933.1:g.5516G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000235345.6:c.132G>T MANE Select | ENSP00000235345.5:p.Leu44= | |
| ENST00000235345.5:c.132G>T | ENSP00000235345.5:p.Leu44= | |
| NM_015139.2:c.132G>T | NP_055954.1:p.Leu44= | |
| XM_006710478.1:c.132G>T | XP_006710541.1:p.Leu44= | |
| XM_011541070.1:c.132G>T | XP_011539372.1:p.Leu44= | |
| XM_006710478.2:c.132G>T | XP_006710541.1:p.Leu44= | |
| XM_011541070.2:c.132G>T | XP_011539372.1:p.Leu44= | |
| XR_001737057.2:n.542G>T | ||
| XR_001737058.2:n.535G>T | ||
| NM_015139.3:c.132G>T MANE Select | NP_055954.1:p.Leu44= |