Linked Data
MyVariant Identifiers:
chr11:g.67352219C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67584748C>T , CM000673.2:g.67584748C>T | GRCh38 |
| NC_000011.9:g.67352219C>T , CM000673.1:g.67352219C>T | GRCh37 |
| NC_000011.8:g.67108795C>T | NCBI36 |
| NG_012075.1:g.6154C>T , LRG_723:g.6154C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.208C>T | ENSP00000381604.1:p.Leu70= | |
| ENST00000398606.10:c.208C>T MANE Select | ENSP00000381607.3:p.Leu70= | |
| ENST00000646888.1:c.101C>T | ENSP00000494477.1:p.Pro34Leu | |
| ENST00000398603.5:c.208C>T | ENSP00000381604.1:p.Leu70= | |
| ENST00000398606.7:c.208C>T | ENSP00000381607.3:p.Leu70= | |
| ENST00000489040.1:n.207C>T | ||
| ENST00000494593.1:n.638C>T | ||
| ENST00000498765.5:c.171C>T | ||
| NM_000852.3:c.208C>T , LRG_723t1:c.208C>T | NP_000843.1:p.Leu70= | |
| NM_000852.4:c.208C>T MANE Select | NP_000843.1:p.Leu70= |