Linked Data
ClinVar Variation Id:
1631217
ClinVar RCV Id:
RCV002123892
dbSNP Id:
rs1321969110
gnomAD v4:
1-2408845-C-G
MyVariant Identifiers:
chr1:g.2340284C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.2408845C>G , CM000663.2:g.2408845C>G | GRCh38 |
| NC_000001.10:g.2340284C>G , CM000663.1:g.2340284C>G | GRCh37 |
| NC_000001.9:g.2330144C>G | NCBI36 |
| NG_008342.1:g.8727G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000288774.8:c.207G>C | ENSP00000288774.3:p.Leu69= | |
| ENST00000447513.7:c.207G>C MANE Select | ENSP00000407922.2:p.Leu69= | |
| ENST00000650293.1:c.161G>C | ||
| ENST00000288774.7:c.207G>C | ENSP00000288774.3:p.Leu69= | |
| ENST00000447513.6:c.207G>C | ENSP00000407922.2:p.Leu69= | |
| ENST00000502666.1:c.412G>C | ENSP00000461951.1:n.412G>C | |
| ENST00000507596.5:c.207G>C | ENSP00000424291.1:p.Leu69= | |
| ENST00000508384.5:c.-226G>C | ENSP00000464289.1:n.-226G>C | |
| ENST00000510434.1:c.207G>C | ENSP00000423051.1:p.Leu69= | |
| ENST00000514502.1:c.*224G>C | ENSP00000425924.1:n.*224G>C | |
| ENST00000515760.1:n.341G>C | ||
| NM_002617.3:c.207G>C | NP_002608.1:p.Leu69= | |
| NM_153818.1:c.207G>C | NP_722540.1:p.Leu69= | |
| XM_011541573.1:c.207G>C | XP_011539875.1:p.Leu69= | |
| XM_011541574.1:c.-226G>C | XP_011539876.1:n.-226G>C | |
| XM_011541575.1:c.-226G>C | XP_011539877.1:n.-226G>C | |
| XM_011541576.1:c.207G>C | XP_011539878.1:p.Leu69= | |
| XR_946666.1:n.327G>C | ||
| XM_011541576.2:c.207G>C | XP_011539878.1:p.Leu69= | |
| XR_946666.2:n.276G>C | ||
| NM_001374425.1:c.207G>C | NP_001361354.1:p.Leu69= | |
| NM_001374426.1:c.-226G>C | NP_001361355.1:n.-226G>C | |
| NM_001374427.1:c.-226G>C | NP_001361356.1:n.-226G>C | |
| NM_002617.4:c.207G>C MANE Select | NP_002608.1:p.Leu69= | |
| NM_153818.2:c.207G>C | NP_722540.1:p.Leu69= | |
| NR_164636.1:n.326G>C |