Linked Data
ClinVar Variation Id:
3227065
ClinVar RCV Id:
RCV004522230
MyVariant Identifiers:
chr2:g.96930964G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.96265226G>A , CM000664.2:g.96265226G>A | GRCh38 |
| NC_000002.11:g.96930964G>A , CM000664.1:g.96930964G>A | GRCh37 |
| NC_000002.10:g.96294691G>A | NCBI36 |
| NG_027695.1:g.5788C>T , LRG_528:g.5788C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258439.8:c.156C>T MANE Select | ENSP00000258439.3:p.Ala52= | |
| ENST00000258439.7:c.156C>T | ENSP00000258439.2:p.Ala52= | |
| ENST00000432959.1:c.156C>T | ENSP00000416660.1:p.Ala52= | |
| NM_001193304.2:c.156C>T | NP_001180233.1:p.Ala52= | |
| NM_017849.3:c.156C>T , LRG_528t1:c.156C>T | NP_060319.1:p.Ala52= | |
| NM_001193304.3:c.156C>T | NP_001180233.1:p.Ala52= | |
| NM_017849.4:c.156C>T MANE Select | NP_060319.1:p.Ala52= |