Linked Data
MyVariant Identifiers:
chr10:g.96522603T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94762846T>A , CM000672.2:g.94762846T>A | GRCh38 |
| NC_000010.10:g.96522603T>A , CM000672.1:g.96522603T>A | GRCh37 |
| NC_000010.9:g.96512593T>A | NCBI36 |
| NG_008384.2:g.5141T>A | |
| NG_008384.3:g.5166T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.141T>A MANE Select | ENSP00000360372.3:p.Ile47= | |
| ENST00000371321.7:c.141T>A | ENSP00000360372.3:p.Ile47= | |
| ENST00000464755.1:c.932-12212T>A | ENSP00000483243.1:n.932-12212T>A | |
| ENST00000480405.2:c.141T>A | ENSP00000483847.1:p.Ile47= | |
| NM_000769.2:c.141T>A | NP_000760.1:p.Ile47= | |
| NM_000769.4:c.141T>A MANE Select | NP_000760.1:p.Ile47= |