Linked Data
gnomAD v4:
1-94046946-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94046946T>C , CM000663.2:g.94046946T>C | GRCh38 |
| NC_000001.10:g.94512502T>C , CM000663.1:g.94512502T>C | GRCh37 |
| NC_000001.9:g.94285090T>C | NCBI36 |
| NG_009073.1:g.79204A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000370225.4:c.2891A>G MANE Select | ENSP00000359245.3:p.His964Arg | |
| ENST00000649773.1:c.2669A>G | ENSP00000496882.1:p.His890Arg | |
| ENST00000370225.3:c.2891A>G | ENSP00000359245.3:p.His964Arg | |
| ENST00000536513.5:c.-64-6857A>G | ENSP00000439707.2:n.-64-6857A>G | |
| NM_000350.2:c.2891A>G | NP_000341.2:p.His964Arg | |
| NM_000350.3:c.2891A>G MANE Select | NP_000341.2:p.His964Arg |