Linked Data
dbSNP Id:
rs2068699547
gnomAD v4:
3-128486340-G-T
MyVariant Identifiers:
chr3:g.128205183G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.128486340G>T , CM000665.2:g.128486340G>T | GRCh38 |
| NC_000003.11:g.128205183G>T , CM000665.1:g.128205183G>T | GRCh37 |
| NC_000003.10:g.129687873G>T | NCBI36 |
| NG_029334.1:g.11848C>A , LRG_295:g.11848C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000487848.6:c.258C>A MANE Plus Clinical | ENSP00000417074.1:p.Arg86= | |
| ENST00000696466.1:c.540C>A | ENSP00000512647.1:p.Arg180= | |
| ENST00000341105.7:c.258C>A MANE Select | ENSP00000345681.2:p.Arg86= | |
| ENST00000341105.6:c.258C>A | ENSP00000345681.2:p.Arg86= | |
| ENST00000430265.6:c.258C>A | ENSP00000400259.2:p.Arg86= | |
| ENST00000487848.5:c.258C>A | ENSP00000417074.1:p.Arg86= | |
| ENST00000492608.1:c.258C>A | ENSP00000418132.1:p.Arg86= | |
| NM_001145661.1:c.258C>A , LRG_295t1:c.258C>A | NP_001139133.1:p.Arg86= | |
| NM_001145662.1:c.258C>A | NP_001139134.1:p.Arg86= | |
| NM_032638.4:c.258C>A , LRG_295t2:c.258C>A | NP_116027.2:p.Arg86= | |
| NM_001145661.2:c.258C>A MANE Plus Clinical | NP_001139133.1:p.Arg86= | |
| NM_032638.5:c.258C>A MANE Select | NP_116027.2:p.Arg86= |