Linked Data
MyVariant Identifiers:
chr11:g.67352158A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67584687A>C , CM000673.2:g.67584687A>C | GRCh38 |
| NC_000011.9:g.67352158A>C , CM000673.1:g.67352158A>C | GRCh37 |
| NC_000011.8:g.67108734A>C | NCBI36 |
| NG_012075.1:g.6093A>C , LRG_723:g.6093A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.147A>C | ENSP00000381604.1:p.Leu49= | |
| ENST00000398606.10:c.147A>C MANE Select | ENSP00000381607.3:p.Leu49= | |
| ENST00000646888.1:c.40A>C | ENSP00000494477.1:p.Ile14Leu | |
| ENST00000398603.5:c.147A>C | ENSP00000381604.1:p.Leu49= | |
| ENST00000398606.7:c.147A>C | ENSP00000381607.3:p.Leu49= | |
| ENST00000489040.1:n.146A>C | ||
| ENST00000494593.1:n.577A>C | ||
| ENST00000498765.5:c.110A>C | ||
| NM_000852.3:c.147A>C , LRG_723t1:c.147A>C | NP_000843.1:p.Leu49= | |
| NM_000852.4:c.147A>C MANE Select | NP_000843.1:p.Leu49= |