Linked Data
MyVariant Identifiers:
chr11:g.47359332T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47337781T>A , CM000673.2:g.47337781T>A | GRCh38 |
| NC_000011.9:g.47359332T>A , CM000673.1:g.47359332T>A | GRCh37 |
| NC_000011.8:g.47315908T>A | NCBI36 |
| NG_007667.1:g.19922A>T , LRG_386:g.19922A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000545968.6:c.2322A>T MANE Select | ENSP00000442795.1:p.Ala774= | |
| ENST00000256993.8:c.2322A>T | ENSP00000256993.5:p.Ala774= | |
| ENST00000399249.6:c.2322A>T | ENSP00000382193.2:p.Ala774= | |
| ENST00000544791.1:c.2322A>T | ENSP00000444259.1:p.Ala774= | |
| ENST00000545968.5:c.2322A>T | ENSP00000442795.1:p.Ala774= | |
| NM_000256.3:c.2322A>T , LRG_386t1:c.2322A>T MANE Select | NP_000247.2:p.Ala774= | |
| XM_011520117.1:c.2304A>T | XP_011518419.1:p.Ala768= | |
| XM_011520118.1:c.2241A>T | XP_011518420.1:p.Ala747= |