Linked Data
ClinVar Variation Id:
2883790
ClinVar RCV Id:
RCV003606649
MyVariant Identifiers:
chr1:g.55509677G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55044004G>A , CM000663.2:g.55044004G>A | GRCh38 |
| NC_000001.10:g.55509677G>A , CM000663.1:g.55509677G>A | GRCh37 |
| NC_000001.9:g.55282265G>A | NCBI36 |
| NG_009061.1:g.9458G>A , LRG_275:g.9458G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.369G>A | ENSP00000501161.2:p.Leu123= | |
| ENST00000710286.1:c.726G>A | ENSP00000518176.1:p.Leu242= | |
| ENST00000673662.1:n.39G>A | ||
| ENST00000673726.1:c.369G>A | ENSP00000501004.1:p.Leu123= | |
| ENST00000673903.1:c.-7G>A | ENSP00000501257.1:n.-7G>A | |
| ENST00000302118.5:c.369G>A MANE Select | ENSP00000303208.5:p.Leu123= | |
| NM_174936.3:c.369G>A , LRG_275t1:c.369G>A | NP_777596.2:p.Leu123= | |
| NR_110451.1:n.182+3601G>A | ||
| NM_174936.4:c.369G>A MANE Select | NP_777596.2:p.Leu123= | |
| NR_110451.2:n.182+3601G>A |