Linked Data
MyVariant Identifiers:
chr11:g.69462889C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.69648121C>A , CM000673.2:g.69648121C>A | GRCh38 |
| NC_000011.9:g.69462889C>A , CM000673.1:g.69462889C>A | GRCh37 |
| NC_000011.8:g.69172070C>A | NCBI36 |
| NG_007375.1:g.12017C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227507.3:c.702C>A MANE Select | ENSP00000227507.2:p.Ser234= | |
| ENST00000227507.2:c.702C>A | ENSP00000227507.2:p.Ser234= | |
| ENST00000536559.1:c.*122C>A | ENSP00000438482.1:n.*122C>A | |
| ENST00000542367.1:n.165C>A | ||
| ENST00000545484.1:n.408C>A | ||
| NM_053056.2:c.702C>A | NP_444284.1:p.Ser234= | |
| XM_006718653.2:c.726C>A | XP_006718716.1:p.Ser242= | |
| NM_053056.3:c.702C>A MANE Select | NP_444284.1:p.Ser234= |