Linked Data
MyVariant Identifiers:
chr11:g.112097214C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112226491C>G , CM000673.2:g.112226491C>G | GRCh38 |
| NC_000011.9:g.112097214C>G , CM000673.1:g.112097214C>G | GRCh37 |
| NC_000011.8:g.111602424C>G | NCBI36 |
| NG_008743.1:g.5127C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000280362.8:c.48C>G MANE Select | ENSP00000280362.3:p.Arg16= | |
| ENST00000280362.7:c.48C>G | ENSP00000280362.3:p.Arg16= | |
| ENST00000525645.1:n.123C>G | ||
| ENST00000525803.1:c.48C>G | ENSP00000431750.1:p.Arg16= | |
| ENST00000528679.5:c.48C>G | ENSP00000435895.1:p.Arg16= | |
| ENST00000531673.5:c.48C>G | ENSP00000433469.1:p.Arg16= | |
| NM_000317.2:c.48C>G | NP_000308.1:p.Arg16= | |
| NM_000317.3:c.48C>G MANE Select | NP_000308.1:p.Arg16= |