Linked Data
MyVariant Identifiers:
chr11:g.67353913A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67586442A>T , CM000673.2:g.67586442A>T | GRCh38 |
| NC_000011.9:g.67353913A>T , CM000673.1:g.67353913A>T | GRCh37 |
| NC_000011.8:g.67110489A>T | NCBI36 |
| NG_012075.1:g.7848A>T , LRG_723:g.7848A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.390A>T | ENSP00000381604.1:p.Leu130= | |
| ENST00000398606.10:c.498A>T MANE Select | ENSP00000381607.3:p.Leu166= | |
| ENST00000646888.1:c.*214A>T | ENSP00000494477.1:n.*214A>T | |
| ENST00000398603.5:c.390A>T | ENSP00000381604.1:p.Leu130= | |
| ENST00000398606.7:c.498A>T | ENSP00000381607.3:p.Leu166= | |
| ENST00000467591.1:n.609A>T | ||
| ENST00000494593.1:n.1470A>T | ||
| ENST00000498765.5:c.561A>T | ||
| NM_000852.3:c.498A>T , LRG_723t1:c.498A>T | NP_000843.1:p.Leu166= | |
| NM_000852.4:c.498A>T MANE Select | NP_000843.1:p.Leu166= |