Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94046946T>A , CM000663.2:g.94046946T>A | GRCh38 |
| NC_000001.10:g.94512502T>A , CM000663.1:g.94512502T>A | GRCh37 |
| NC_000001.9:g.94285090T>A | NCBI36 |
| NG_009073.1:g.79204A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370225.4:c.2891A>T MANE Select | ENSP00000359245.3:p.His964Leu | |
| ENST00000649773.1:c.2669A>T | ENSP00000496882.1:p.His890Leu | |
| ENST00000370225.3:c.2891A>T | ENSP00000359245.3:p.His964Leu | |
| ENST00000536513.5:c.-64-6857A>T | ENSP00000439707.2:n.-64-6857A>T | |
| NM_000350.2:c.2891A>T | NP_000341.2:p.His964Leu | |
| NM_000350.3:c.2891A>T MANE Select | NP_000341.2:p.His964Leu |