Linked Data
MyVariant Identifiers:
chr1:g.160851798G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160882008G>A , CM000663.2:g.160882008G>A | GRCh38 |
| NC_000001.10:g.160851798G>A , CM000663.1:g.160851798G>A | GRCh37 |
| NC_000001.9:g.159118422G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326245.4:c.354C>T MANE Select | ENSP00000323587.3:p.Ala118= | |
| ENST00000326245.3:c.354C>T | ENSP00000323587.3:p.Ala118= | |
| ENST00000464077.1:n.288C>T | ||
| NM_017625.2:c.354C>T | NP_060095.2:p.Ala118= | |
| NM_017625.3:c.354C>T MANE Select | NP_060095.2:p.Ala118= |