Linked Data
MyVariant Identifiers:
chr11:g.22646634A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625088A>T , CM000673.2:g.22625088A>T | GRCh38 |
| NC_000011.9:g.22646634A>T , CM000673.1:g.22646634A>T | GRCh37 |
| NC_000011.8:g.22603210A>T | NCBI36 |
| NG_007425.1:g.5754T>A , LRG_527:g.5754T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327470.6:c.723T>A MANE Select | ENSP00000330875.3:p.Leu241= | |
| ENST00000327470.4:c.723T>A | ENSP00000330875.3:p.Leu241= | |
| NM_022725.3:c.723T>A , LRG_527t1:c.723T>A | NP_073562.1:p.Leu241= | |
| NM_022725.4:c.723T>A MANE Select | NP_073562.1:p.Leu241= |