Linked Data
MyVariant Identifiers:
chr22:g.50659509A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50221080A>T , CM000684.2:g.50221080A>T | GRCh38 |
| NC_000022.10:g.50659509A>T , CM000684.1:g.50659509A>T | GRCh37 |
| NC_000022.9:g.49001636A>T | NCBI36 |
| NG_032160.1:g.28892T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000248846.10:c.3279T>A MANE Select | ENSP00000248846.5:p.Ser1093= | |
| ENST00000248846.9:c.3279T>A | ENSP00000248846.5:p.Ser1093= | |
| ENST00000439308.6:c.3279T>A | ENSP00000397387.2:p.Ser1093= | |
| ENST00000491449.5:n.1586T>A | ||
| ENST00000498611.5:n.3617+195T>A | ||
| NM_020461.3:c.3279T>A | NP_065194.2:p.Ser1093= | |
| XR_938347.1:n.3844T>A | ||
| XR_938348.1:n.3049+948T>A | ||
| XR_001755343.2:n.3848T>A | ||
| XR_001755344.2:n.3848T>A | ||
| XR_002958720.1:n.3053+948T>A | ||
| XR_938347.2:n.3848T>A | ||
| NM_020461.4:c.3279T>A MANE Select | NP_065194.3:p.Ser1093= |