Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94852910T>C , CM000672.2:g.94852910T>C | GRCh38 |
| NC_000010.10:g.96612667T>C , CM000672.1:g.96612667T>C | GRCh37 |
| NC_000010.9:g.96602657T>C | NCBI36 |
| NG_008384.2:g.95205T>C | |
| NG_008384.3:g.95230T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.1469T>C MANE Select | ENSP00000360372.3:p.Val490Ala | |
| ENST00000645461.1:n.2380T>C | ||
| ENST00000371321.7:c.1469T>C | ENSP00000360372.3:p.Val490Ala | |
| ENST00000464755.1:c.2232T>C | ENSP00000483243.1:n.2232T>C | |
| NM_000769.2:c.1469T>C | NP_000760.1:p.Val490Ala | |
| NM_000769.4:c.1469T>C MANE Select | NP_000760.1:p.Val490Ala |