Linked Data
MyVariant Identifiers:
chr22:g.44342130A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43946250A>G , CM000684.2:g.43946250A>G | GRCh38 |
| NC_000022.10:g.44342130A>G , CM000684.1:g.44342130A>G | GRCh37 |
| NC_000022.9:g.42673463A>G | NCBI36 |
| NG_008631.1:g.27512A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.1314A>G MANE Select | ENSP00000216180.3:p.Ala438= | |
| ENST00000216180.7:c.1314A>G | ENSP00000216180.3:p.Ala438= | |
| ENST00000406117.6:c.*849+1455A>G | ENSP00000384668.2:n.*849+1455A>G | |
| ENST00000423180.2:c.1302A>G | ENSP00000397987.2:p.Ala434= | |
| NM_025225.2:c.1314A>G | NP_079501.2:p.Ala438= | |
| NM_025225.3:c.1314A>G MANE Select | NP_079501.2:p.Ala438= |