Linked Data
MyVariant Identifiers:
chr1:g.94512501G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94046945G>A , CM000663.2:g.94046945G>A | GRCh38 |
| NC_000001.10:g.94512501G>A , CM000663.1:g.94512501G>A | GRCh37 |
| NC_000001.9:g.94285089G>A | NCBI36 |
| NG_009073.1:g.79205C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370225.4:c.2892C>T MANE Select | ENSP00000359245.3:p.His964= | |
| ENST00000649773.1:c.2670C>T | ENSP00000496882.1:p.His890= | |
| ENST00000370225.3:c.2892C>T | ENSP00000359245.3:p.His964= | |
| ENST00000536513.5:c.-64-6856C>T | ENSP00000439707.2:n.-64-6856C>T | |
| NM_000350.2:c.2892C>T | NP_000341.2:p.His964= | |
| NM_000350.3:c.2892C>T MANE Select | NP_000341.2:p.His964= |