Linked Data
MyVariant Identifiers:
chr1:g.67519661A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67053978A>T , CM000663.2:g.67053978A>T | GRCh38 |
| NC_000001.10:g.67519661A>T , CM000663.1:g.67519661A>T | GRCh37 |
| NC_000001.9:g.67292249A>T | NCBI36 |
| NG_012933.1:g.5420T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000235345.6:c.36T>A MANE Select | ENSP00000235345.5:p.Val12= | |
| ENST00000235345.5:c.36T>A | ENSP00000235345.5:p.Val12= | |
| NM_015139.2:c.36T>A | NP_055954.1:p.Val12= | |
| XM_006710478.1:c.36T>A | XP_006710541.1:p.Val12= | |
| XM_011541070.1:c.36T>A | XP_011539372.1:p.Val12= | |
| XM_006710478.2:c.36T>A | XP_006710541.1:p.Val12= | |
| XM_011541070.2:c.36T>A | XP_011539372.1:p.Val12= | |
| XR_001737057.2:n.446T>A | ||
| XR_001737058.2:n.439T>A | ||
| NM_015139.3:c.36T>A MANE Select | NP_055954.1:p.Val12= |