Linked Data
MyVariant Identifiers:
chr11:g.118183352T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312637T>A , CM000673.2:g.118312637T>A | GRCh38 |
| NC_000011.9:g.118183352T>A , CM000673.1:g.118183352T>A | GRCh37 |
| NC_000011.8:g.117688562T>A | NCBI36 |
| NG_007383.1:g.13058T>A , LRG_38:g.13058T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.123T>A MANE Select | ENSP00000354566.4:p.Ser41= | |
| ENST00000361763.8:c.123T>A | ENSP00000354566.4:p.Ser41= | |
| ENST00000526146.5:n.669T>A | ||
| ENST00000528435.5:n.676T>A | ||
| ENST00000528600.1:c.105T>A | ENSP00000433975.1:p.Ser35= | |
| ENST00000529713.5:n.229T>A | ||
| ENST00000531913.1:n.494T>A | ||
| NM_000733.3:c.123T>A , LRG_38t1:c.123T>A | NP_000724.1:p.Ser41= | |
| NM_000733.4:c.123T>A MANE Select | NP_000724.1:p.Ser41= |