Linked Data
MyVariant Identifiers:
chr11:g.69462839A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.69648071A>C , CM000673.2:g.69648071A>C | GRCh38 |
| NC_000011.9:g.69462839A>C , CM000673.1:g.69462839A>C | GRCh37 |
| NC_000011.8:g.69172020A>C | NCBI36 |
| NG_007375.1:g.11967A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227507.3:c.652A>C MANE Select | ENSP00000227507.2:p.Arg218= | |
| ENST00000227507.2:c.652A>C | ENSP00000227507.2:p.Arg218= | |
| ENST00000536559.1:c.*72A>C | ENSP00000438482.1:n.*72A>C | |
| ENST00000542367.1:n.115A>C | ||
| ENST00000545484.1:n.358A>C | ||
| NM_053056.2:c.652A>C | NP_444284.1:p.Arg218= | |
| XM_006718653.2:c.676A>C | XP_006718716.1:p.Arg226= | |
| NM_053056.3:c.652A>C MANE Select | NP_444284.1:p.Arg218= |