Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31667263T>C , CM000683.2:g.31667263T>C | GRCh38 |
| NC_000021.8:g.33039576T>C , CM000683.1:g.33039576T>C | GRCh37 |
| NC_000021.7:g.31961447T>C | NCBI36 |
| NG_008689.1:g.12642T>C , LRG_652:g.12642T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.11:c.245T>C MANE Select | ENSP00000270142.7:p.Val82Ala | |
| ENST00000270142.10:c.245T>C | ENSP00000270142.6:p.Val82Ala | |
| ENST00000389995.4:c.188T>C | ENSP00000374645.4:p.Val63Ala | |
| ENST00000470944.1:n.1173T>C | ||
| ENST00000476106.5:n.508T>C | ||
| NM_000454.4:c.245T>C , LRG_652t1:c.245T>C | NP_000445.1:p.Val82Ala | |
| NM_000454.5:c.245T>C MANE Select | NP_000445.1:p.Val82Ala |