Linked Data
ClinVar Variation Id:
1673709
ClinVar RCV Id:
RCV002214047
dbSNP Id:
rs2106011547
MyVariant Identifiers:
chr2:g.219746953C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218882231C>T , CM000664.2:g.218882231C>T | GRCh38 |
| NC_000002.11:g.219746953C>T , CM000664.1:g.219746953C>T | GRCh37 |
| NC_000002.10:g.219455197C>T | NCBI36 |
| NG_012179.1:g.6699C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.184C>T MANE Select | ENSP00000258411.3:p.Leu62= | |
| ENST00000258411.7:c.184C>T | ENSP00000258411.3:p.Leu62= | |
| ENST00000458582.1:c.71C>T | ||
| NM_025216.2:c.184C>T | NP_079492.2:p.Leu62= | |
| XM_011511928.1:c.133C>T | XP_011510230.1:p.Leu45= | |
| XM_011511929.1:c.88C>T | XP_011510231.1:p.Leu30= | |
| XM_011511930.1:c.184C>T | XP_011510232.1:p.Leu62= | |
| XM_011511929.2:c.88C>T | XP_011510231.1:p.Leu30= | |
| NM_025216.3:c.184C>T MANE Select | NP_079492.2:p.Leu62= |