Linked Data
MyVariant Identifiers:
chr11:g.22646580A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625034A>G , CM000673.2:g.22625034A>G | GRCh38 |
| NC_000011.9:g.22646580A>G , CM000673.1:g.22646580A>G | GRCh37 |
| NC_000011.8:g.22603156A>G | NCBI36 |
| NG_007425.1:g.5808T>C , LRG_527:g.5808T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327470.6:c.777T>C MANE Select | ENSP00000330875.3:p.Leu259= | |
| ENST00000327470.4:c.777T>C | ENSP00000330875.3:p.Leu259= | |
| NM_022725.3:c.777T>C , LRG_527t1:c.777T>C | NP_073562.1:p.Leu259= | |
| NM_022725.4:c.777T>C MANE Select | NP_073562.1:p.Leu259= |