Linked Data
MyVariant Identifiers:
chr1:g.165389144A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.165419907A>T , CM000663.2:g.165419907A>T | GRCh38 |
| NC_000001.10:g.165389144A>T , CM000663.1:g.165389144A>T | GRCh37 |
| NC_000001.9:g.163655768A>T | NCBI36 |
| NG_029517.1:g.30449T>A | |
| NG_029517.2:g.30449T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359842.10:c.405T>A MANE Select | ENSP00000352900.5:p.Val135= | |
| ENST00000359842.9:c.405T>A | ENSP00000352900.5:p.Val135= | |
| ENST00000470566.1:n.330T>A | ||
| ENST00000619224.1:c.36T>A | ENSP00000482458.1:p.Val12= | |
| NM_001256570.1:c.36T>A | NP_001243499.1:p.Val12= | |
| NM_001256571.1:c.36T>A | NP_001243500.1:p.Val12= | |
| NM_006917.4:c.405T>A | NP_008848.1:p.Val135= | |
| NM_006917.5:c.405T>A MANE Select | NP_008848.1:p.Val135= | |
| NM_001256571.2:c.36T>A | NP_001243500.1:p.Val12= | |
| NM_001256570.2:c.36T>A | NP_001243499.1:p.Val12= |