Linked Data
MyVariant Identifiers:
chr22:g.44342136C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43946256C>A , CM000684.2:g.43946256C>A | GRCh38 |
| NC_000022.10:g.44342136C>A , CM000684.1:g.44342136C>A | GRCh37 |
| NC_000022.9:g.42673469C>A | NCBI36 |
| NG_008631.1:g.27518C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.1320C>A MANE Select | ENSP00000216180.3:p.Thr440= | |
| ENST00000216180.7:c.1320C>A | ENSP00000216180.3:p.Thr440= | |
| ENST00000406117.6:c.*849+1461C>A | ENSP00000384668.2:n.*849+1461C>A | |
| ENST00000423180.2:c.1308C>A | ENSP00000397987.2:p.Thr436= | |
| NM_025225.2:c.1320C>A | NP_079501.2:p.Thr440= | |
| NM_025225.3:c.1320C>A MANE Select | NP_079501.2:p.Thr440= |