Linked Data
MyVariant Identifiers:
chr22:g.32500775C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32104788C>A , CM000684.2:g.32104788C>A | GRCh38 |
| NC_000022.10:g.32500775C>A , CM000684.1:g.32500775C>A | GRCh37 |
| NC_000022.9:g.30830775C>A | NCBI36 |
| NG_017045.1:g.66757C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266088.9:c.1668C>A MANE Select | ENSP00000266088.4:p.Leu556= | |
| ENST00000266088.8:c.1668C>A | ENSP00000266088.4:p.Leu556= | |
| ENST00000543737.2:c.1287C>A | ENSP00000444898.1:p.Leu429= | |
| NM_000343.3:c.1668C>A | NP_000334.1:p.Leu556= | |
| NM_001256314.1:c.1287C>A | NP_001243243.1:p.Leu429= | |
| XR_938173.1:n.591+2050G>T | ||
| XR_938174.1:n.486+15067G>T | ||
| NM_000343.4:c.1668C>A MANE Select | NP_000334.1:p.Leu556= | |
| NM_001256314.2:c.1287C>A | NP_001243243.1:p.Leu429= |