Linked Data
ClinVar Variation Id:
2119675
ClinVar RCV Id:
RCV003033212
MyVariant Identifiers:
chr2:g.28999820G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.28776954G>A , CM000664.2:g.28776954G>A | GRCh38 |
| NC_000002.11:g.28999820G>A , CM000664.1:g.28999820G>A | GRCh37 |
| NC_000002.10:g.28853324G>A | NCBI36 |
| NG_052878.1:g.30207G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000418910.2:c.156G>A | ENSP00000388056.2:p.Leu52= | |
| ENST00000420282.6:c.156G>A | ENSP00000398839.2:p.Leu52= | |
| ENST00000427786.2:c.72G>A | ENSP00000394589.1:p.Leu24= | |
| ENST00000441461.6:c.156G>A | ENSP00000414918.2:p.Leu52= | |
| ENST00000455580.6:c.72G>A | ENSP00000390715.2:p.Leu24= | |
| ENST00000703171.1:c.156G>A | ENSP00000515217.1:p.Leu52= | |
| ENST00000703172.1:c.72G>A | ENSP00000515218.1:p.Leu24= | |
| ENST00000703173.1:c.156G>A | ENSP00000515219.1:p.Leu52= | |
| ENST00000703174.1:c.156G>A | ENSP00000515220.1:p.Leu52= | |
| ENST00000703176.1:c.123G>A | ENSP00000515221.1:p.Leu41= | |
| ENST00000703177.1:c.72G>A | ENSP00000515222.1:p.Leu24= | |
| ENST00000395366.3:c.156G>A MANE Select | ENSP00000378769.2:p.Leu52= | |
| ENST00000296122.10:c.156G>A | ENSP00000296122.6:p.Leu52= | |
| ENST00000358506.6:c.156G>A | ENSP00000351298.2:p.Leu52= | |
| ENST00000395366.2:c.156G>A | ENSP00000378769.2:p.Leu52= | |
| ENST00000420282.5:c.156G>A | ENSP00000398839.1:p.Leu52= | |
| ENST00000427786.1:c.72G>A | ENSP00000394589.1:p.Leu24= | |
| ENST00000441461.5:c.156G>A | ENSP00000414918.1:p.Leu52= | |
| ENST00000455580.5:c.72G>A | ENSP00000390715.1:p.Leu24= | |
| ENST00000464273.1:n.270G>A | ||
| NM_002709.2:c.156G>A | NP_002700.1:p.Leu52= | |
| NM_206876.1:c.156G>A | NP_996759.1:p.Leu52= | |
| NM_002709.3:c.156G>A MANE Select | NP_002700.1:p.Leu52= | |
| NM_206876.2:c.156G>A | NP_996759.1:p.Leu52= |