Linked Data
MyVariant Identifiers:
chr3:g.9932466G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.9890782G>A , CM000665.2:g.9890782G>A | GRCh38 |
| NC_000003.11:g.9932466G>A , CM000665.1:g.9932466G>A | GRCh37 |
| NC_000003.10:g.9907466G>A | NCBI36 |
| NG_041779.1:g.5196G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000489724.2:c.60G>A | ENSP00000497724.1:p.Arg20= | |
| ENST00000647897.1:c.60G>A MANE Select | ENSP00000496942.1:p.Arg20= | |
| ENST00000307768.4:c.60G>A | ENSP00000306106.4:p.Arg20= | |
| ENST00000489724.1:n.150G>A | ||
| ENST00000616966.2:c.60G>A | ENSP00000481606.1:p.Arg20= | |
| NM_032492.3:c.60G>A | NP_115881.3:p.Arg20= | |
| NM_001363890.1:c.-209G>A | NP_001350819.1:n.-209G>A | |
| NM_032492.4:c.60G>A MANE Select | NP_115881.3:p.Arg20= |