Linked Data
MyVariant Identifiers:
chr22:g.20230074G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.20242551G>T , CM000684.2:g.20242551G>T | GRCh38 |
| NC_000022.10:g.20230074G>T , CM000684.1:g.20230074G>T | GRCh37 |
| NC_000022.9:g.18610074G>T | NCBI36 |
| NG_012176.1:g.30743C>A | |
| NG_012176.2:g.30743C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000043402.8:c.582C>A MANE Select | ENSP00000043402.7:p.Pro194= | |
| ENST00000043402.7:c.582C>A | ENSP00000043402.7:p.Pro194= | |
| ENST00000416372.5:c.641C>A | ||
| ENST00000425986.1:c.839C>A | ||
| NM_023004.5:c.582C>A | NP_075380.1:p.Pro194= | |
| NM_023004.6:c.582C>A MANE Select | NP_075380.1:p.Pro194= |