Linked Data
MyVariant Identifiers:
chr10:g.96522612C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94762855C>T , CM000672.2:g.94762855C>T | GRCh38 |
| NC_000010.10:g.96522612C>T , CM000672.1:g.96522612C>T | GRCh37 |
| NC_000010.9:g.96512602C>T | NCBI36 |
| NG_008384.2:g.5150C>T | |
| NG_008384.3:g.5175C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.150C>T MANE Select | ENSP00000360372.3:p.Val50= | |
| ENST00000371321.7:c.150C>T | ENSP00000360372.3:p.Val50= | |
| ENST00000464755.1:c.932-12203C>T | ENSP00000483243.1:n.932-12203C>T | |
| ENST00000480405.2:c.150C>T | ENSP00000483847.1:p.Val50= | |
| NM_000769.2:c.150C>T | NP_000760.1:p.Val50= | |
| NM_000769.4:c.150C>T MANE Select | NP_000760.1:p.Val50= |