Linked Data
MyVariant Identifiers:
chr10:g.96708996C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94949239C>T , CM000672.2:g.94949239C>T | GRCh38 |
| NC_000010.10:g.96708996C>T , CM000672.1:g.96708996C>T | GRCh37 |
| NC_000010.9:g.96698986C>T | NCBI36 |
| NG_008385.1:g.15582C>T | |
| NG_008385.2:g.16082C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.774C>T MANE Select | ENSP00000260682.6:p.Asn258= | |
| ENST00000643112.1:c.774C>T | ENSP00000496202.1:p.Asn258= | |
| ENST00000260682.6:c.774C>T | ENSP00000260682.6:p.Asn258= | |
| ENST00000473496.1:n.545C>T | ||
| NM_000771.3:c.774C>T | NP_000762.2:p.Asn258= | |
| NM_000771.4:c.774C>T MANE Select | NP_000762.2:p.Asn258= |