Linked Data
ClinVar Variation Id:
2795345
ClinVar RCV Id:
RCV003606022
MyVariant Identifiers:
chr1:g.55527175C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55061502C>G , CM000663.2:g.55061502C>G | GRCh38 |
| NC_000001.10:g.55527175C>G , CM000663.1:g.55527175C>G | GRCh37 |
| NC_000001.9:g.55299763C>G | NCBI36 |
| NG_009061.1:g.26956C>G , LRG_275:g.26956C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.*149C>G | ENSP00000501161.2:n.*149C>G | |
| ENST00000710286.1:c.2166C>G | ENSP00000518176.1:p.Ala722= | |
| ENST00000673903.1:c.1434C>G | ENSP00000501257.1:p.Ala478= | |
| ENST00000673913.1:c.659C>G | ENSP00000501161.1:n.659C>G | |
| ENST00000302118.5:c.1809C>G MANE Select | ENSP00000303208.5:p.Ala603= | |
| ENST00000490692.1:n.2355C>G | ||
| NM_174936.3:c.1809C>G , LRG_275t1:c.1809C>G | NP_777596.2:p.Ala603= | |
| NR_110451.1:n.1416C>G | ||
| XM_011541193.1:c.930C>G | XP_011539495.1:p.Ala310= | |
| NM_174936.4:c.1809C>G MANE Select | NP_777596.2:p.Ala603= | |
| NR_110451.2:n.1416C>G |