Linked Data
MyVariant Identifiers:
chr10:g.96541649T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94781892T>A , CM000672.2:g.94781892T>A | GRCh38 |
| NC_000010.10:g.96541649T>A , CM000672.1:g.96541649T>A | GRCh37 |
| NC_000010.9:g.96531639T>A | NCBI36 |
| NG_008384.2:g.24187T>A | |
| NG_008384.3:g.24212T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.714T>A MANE Select | ENSP00000360372.3:p.Ala238= | |
| ENST00000645461.1:n.1767T>A | ||
| ENST00000371321.7:c.714T>A | ENSP00000360372.3:p.Ala238= | |
| ENST00000464755.1:c.1477T>A | ENSP00000483243.1:n.1477T>A | |
| NM_000769.2:c.714T>A | NP_000760.1:p.Ala238= | |
| NM_000769.4:c.714T>A MANE Select | NP_000760.1:p.Ala238= |