Linked Data
MyVariant Identifiers:
chr10:g.96702073T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94942316T>C , CM000672.2:g.94942316T>C | GRCh38 |
| NC_000010.10:g.96702073T>C , CM000672.1:g.96702073T>C | GRCh37 |
| NC_000010.9:g.96692063T>C | NCBI36 |
| NG_008385.1:g.8659T>C | |
| NG_008385.2:g.9159T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.456T>C MANE Select | ENSP00000260682.6:p.Leu152= | |
| ENST00000643112.1:c.456T>C | ENSP00000496202.1:p.Leu152= | |
| ENST00000645207.1:n.609T>C | ||
| ENST00000260682.6:c.456T>C | ENSP00000260682.6:p.Leu152= | |
| ENST00000461906.1:n.481T>C | ||
| ENST00000473496.1:n.227T>C | ||
| NM_000771.3:c.456T>C | NP_000762.2:p.Leu152= | |
| NM_000771.4:c.456T>C MANE Select | NP_000762.2:p.Leu152= |