Linked Data
MyVariant Identifiers:
chr22:g.32445914A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32049927A>T , CM000684.2:g.32049927A>T | GRCh38 |
| NC_000022.10:g.32445914A>T , CM000684.1:g.32445914A>T | GRCh37 |
| NC_000022.9:g.30775914A>T | NCBI36 |
| NG_017045.1:g.11896A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266088.9:c.136-16A>T MANE Select | ENSP00000266088.4:n.136-16A>T | |
| ENST00000266088.8:c.136-16A>T | ENSP00000266088.4:n.136-16A>T | |
| NM_000343.3:c.136-16A>T | NP_000334.1:n.136-16A>T | |
| XM_011530331.1:c.136-16A>T | XP_011528633.1:n.136-16A>T | |
| NM_000343.4:c.136-16A>T MANE Select | NP_000334.1:n.136-16A>T |