Linked Data
MyVariant Identifiers:
chr10:g.96612641C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94852884C>A , CM000672.2:g.94852884C>A | GRCh38 |
| NC_000010.10:g.96612641C>A , CM000672.1:g.96612641C>A | GRCh37 |
| NC_000010.9:g.96602631C>A | NCBI36 |
| NG_008384.2:g.95179C>A | |
| NG_008384.3:g.95204C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.1443C>A MANE Select | ENSP00000360372.3:p.Pro481= | |
| ENST00000645461.1:n.2354C>A | ||
| ENST00000371321.7:c.1443C>A | ENSP00000360372.3:p.Pro481= | |
| ENST00000464755.1:c.2206C>A | ENSP00000483243.1:n.2206C>A | |
| NM_000769.2:c.1443C>A | NP_000760.1:p.Pro481= | |
| NM_000769.4:c.1443C>A MANE Select | NP_000760.1:p.Pro481= |