Linked Data
MyVariant Identifiers:
chr10:g.96701956T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94942199T>C , CM000672.2:g.94942199T>C | GRCh38 |
| NC_000010.10:g.96701956T>C , CM000672.1:g.96701956T>C | GRCh37 |
| NC_000010.9:g.96691946T>C | NCBI36 |
| NG_008385.1:g.8542T>C | |
| NG_008385.2:g.9042T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260682.8:c.339T>C MANE Select | ENSP00000260682.6:p.Val113= | |
| ENST00000643112.1:c.339T>C | ENSP00000496202.1:p.Val113= | |
| ENST00000645207.1:n.492T>C | ||
| ENST00000260682.6:c.339T>C | ENSP00000260682.6:p.Val113= | |
| ENST00000461906.1:n.364T>C | ||
| ENST00000473496.1:n.110T>C | ||
| NM_000771.3:c.339T>C | NP_000762.2:p.Val113= | |
| NM_000771.4:c.339T>C MANE Select | NP_000762.2:p.Val113= |