Linked Data
ClinVar Variation Id:
2760018
ClinVar RCV Id:
RCV003504966
gnomAD v4:
3-33114311-C-T
MyVariant Identifiers:
chr3:g.33155803C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33114311C>T , CM000665.2:g.33114311C>T | GRCh38 |
| NC_000003.11:g.33155803C>T , CM000665.1:g.33155803C>T | GRCh37 |
| NC_000003.10:g.33130807C>T | NCBI36 |
| NG_008122.1:g.5354C>T , LRG_4:g.5354C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320954.11:c.234C>T MANE Select | ENSP00000323696.5:p.Arg78= | |
| ENST00000320954.10:c.234C>T | ENSP00000323696.5:p.Arg78= | |
| ENST00000449224.1:c.234C>T | ENSP00000409997.1:p.Arg78= | |
| NM_006371.4:c.234C>T , LRG_4t1:c.234C>T | NP_006362.1:p.Arg78= | |
| NM_006371.5:c.234C>T MANE Select | NP_006362.1:p.Arg78= | |
| NM_001393363.1:c.234C>T | NP_001380292.1:p.Arg78= | |
| NM_001393364.1:c.234C>T | NP_001380293.1:p.Arg78= | |
| NM_001393365.1:c.234C>T | NP_001380294.1:p.Arg78= |