Linked Data
ClinVar Variation Id:
2729997
ClinVar RCV Id:
RCV003578079
gnomAD v4:
17-47283455-A-T
MyVariant Identifiers:
chr17:g.45360821A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47283455A>T , CM000679.2:g.47283455A>T | GRCh38 |
| NC_000017.10:g.45360821A>T , CM000679.1:g.45360821A>T | GRCh37 |
| NC_000017.9:g.42715820A>T | NCBI36 |
| NG_008332.2:g.34614A>T , LRG_481:g.34614A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696963.1:c.267A>T | ENSP00000513002.1:p.Val89= | |
| ENST00000559488.7:c.267A>T MANE Select | ENSP00000452786.2:p.Val89= | |
| ENST00000559488.5:c.267A>T | ENSP00000452786.1:p.Val89= | |
| ENST00000560629.1:c.232A>T | ||
| ENST00000571680.1:c.267A>T | ENSP00000461626.1:p.Val89= | |
| NM_000212.2:c.267A>T , LRG_481t1:c.267A>T | NP_000203.2:p.Val89= | |
| NM_000212.3:c.267A>T MANE Select | NP_000203.2:p.Val89= |