Linked Data
MyVariant Identifiers:
chr1:g.160851930A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160882140A>T , CM000663.2:g.160882140A>T | GRCh38 |
| NC_000001.10:g.160851930A>T , CM000663.1:g.160851930A>T | GRCh37 |
| NC_000001.9:g.159118554A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326245.4:c.222T>A MANE Select | ENSP00000323587.3:p.Ser74= | |
| ENST00000326245.3:c.222T>A | ENSP00000323587.3:p.Ser74= | |
| ENST00000464077.1:n.156T>A | ||
| NM_017625.2:c.222T>A | NP_060095.2:p.Ser74= | |
| NM_017625.3:c.222T>A MANE Select | NP_060095.2:p.Ser74= |