Linked Data
MyVariant Identifiers:
chr11:g.22646610A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22625064A>C , CM000673.2:g.22625064A>C | GRCh38 |
| NC_000011.9:g.22646610A>C , CM000673.1:g.22646610A>C | GRCh37 |
| NC_000011.8:g.22603186A>C | NCBI36 |
| NG_007425.1:g.5778T>G , LRG_527:g.5778T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327470.6:c.747T>G MANE Select | ENSP00000330875.3:p.Ala249= | |
| ENST00000327470.4:c.747T>G | ENSP00000330875.3:p.Ala249= | |
| NM_022725.3:c.747T>G , LRG_527t1:c.747T>G | NP_073562.1:p.Ala249= | |
| NM_022725.4:c.747T>G MANE Select | NP_073562.1:p.Ala249= |