Linked Data
MyVariant Identifiers:
chr11:g.1075710A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1075710A>G , CM000673.2:g.1075710A>G | GRCh38 |
| NC_000011.9:g.1075710A>G , CM000673.1:g.1075710A>G | GRCh37 |
| NC_000011.8:g.1065710A>G | NCBI36 |
| NG_051929.1:g.5836A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361558.7:n.163A>G | ||
| ENST00000675028.1:c.136A>G | ENSP00000502432.1:p.Lys46Glu | |
| NM_002457.3:c.136A>G | NP_002448.3:p.Lys46Glu | |
| NM_002457.4:c.136A>G | NP_002448.4:p.Lys46Glu |