Linked Data
MyVariant Identifiers:
chr10:g.135352378T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133538874T>C , CM000672.2:g.133538874T>C | GRCh38 |
| NC_000010.10:g.135352378T>C , CM000672.1:g.135352378T>C | GRCh37 |
| NC_000010.9:g.135202368T>C | NCBI36 |
| NG_008383.1:g.16512T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252945.8:c.1392T>C MANE Select | ENSP00000252945.3:p.Val464= | |
| ENST00000252945.7:c.1392T>C | ENSP00000252945.3:p.Val464= | |
| ENST00000368520.1:n.1358+982T>C | ||
| ENST00000463117.6:c.1392T>C | ENSP00000440689.1:p.Val464= | |
| ENST00000469258.1:n.488T>C | ||
| NM_000773.3:c.1392T>C | NP_000764.1:p.Val464= | |
| NM_000773.4:c.1392T>C MANE Select | NP_000764.1:p.Val464= |