Linked Data
ClinVar Variation Id:
1963651
ClinVar RCV Id:
RCV002716056
dbSNP Id:
rs2058615318
gnomAD v4:
18-23535490-T-C
MyVariant Identifiers:
chr18:g.21115454T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.23535490T>C , CM000680.2:g.23535490T>C | GRCh38 |
| NC_000018.9:g.21115454T>C , CM000680.1:g.21115454T>C | GRCh37 |
| NC_000018.8:g.19369452T>C | NCBI36 |
| NG_012795.1:g.56128A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000269228.10:c.3456A>G MANE Select | ENSP00000269228.4:p.Val1152= | |
| ENST00000269228.9:c.3456A>G | ENSP00000269228.4:p.Val1152= | |
| ENST00000586150.5:c.211A>G | ||
| ENST00000588867.1:n.211A>G | ||
| ENST00000591051.1:c.2534A>G | ||
| ENST00000591107.6:c.133A>G | ||
| NM_000271.4:c.3456A>G | NP_000262.2:p.Val1152= | |
| XM_005258277.1:c.3507A>G | XP_005258334.1:p.Val1169= | |
| XM_005258278.3:c.3507A>G | XP_005258335.1:p.Val1169= | |
| XM_005258279.1:c.3456A>G | XP_005258336.1:p.Val1152= | |
| XM_006722479.2:c.3507A>G | XP_006722542.1:p.Val1169= | |
| XM_011526015.1:c.3042A>G | XP_011524317.1:p.Val1014= | |
| XM_005258278.5:c.3507A>G | XP_005258335.1:p.Val1169= | |
| XM_005258279.2:c.3456A>G | XP_005258336.1:p.Val1152= | |
| XM_006722479.3:c.3507A>G | XP_006722542.1:p.Val1169= | |
| XM_017025784.1:c.3507A>G | XP_016881273.1:p.Val1169= | |
| XM_017025785.1:c.3507A>G | XP_016881274.1:p.Val1169= | |
| XM_017025786.1:c.3456A>G | XP_016881275.1:p.Val1152= | |
| XM_017025787.1:c.3456A>G | XP_016881276.1:p.Val1152= | |
| NM_000271.5:c.3456A>G MANE Select | NP_000262.2:p.Val1152= |