Linked Data
ClinVar Variation Id:
2145969
ClinVar RCV Id:
RCV003074324
dbSNP Id:
rs559206877
gnomAD v4:
3-8745813-G-T
MyVariant Identifiers:
chr3:g.8787499G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8745813G>T , CM000665.2:g.8745813G>T | GRCh38 |
| NC_000003.11:g.8787499G>T , CM000665.1:g.8787499G>T | GRCh37 |
| NC_000003.10:g.8762499G>T | NCBI36 |
| NG_008797.2:g.17004G>T , LRG_329:g.17004G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343849.3:c.402G>T MANE Select | ENSP00000341940.2:p.Ala134= | |
| ENST00000343849.2:c.402G>T | ENSP00000341940.2:p.Ala134= | |
| ENST00000397368.2:c.402G>T | ENSP00000380525.2:p.Ala134= | |
| ENST00000472766.1:n.155+11823G>T | ||
| NM_001234.4:c.402G>T | NP_001225.1:p.Ala134= | |
| NM_033337.2:c.402G>T , LRG_329t1:c.402G>T | NP_203123.1:p.Ala134= | |
| NM_001234.5:c.402G>T | NP_001225.1:p.Ala134= | |
| NM_033337.3:c.402G>T MANE Select | NP_203123.1:p.Ala134= |