Linked Data
ClinVar Variation Id:
1558906
ClinVar RCV Id:
RCV002200309
dbSNP Id:
rs767972481
gnomAD v4:
8-43193771-C-G
MyVariant Identifiers:
chr8:g.43048914C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.43193771C>G , CM000670.2:g.43193771C>G | GRCh38 |
| NC_000008.10:g.43048914C>G , CM000670.1:g.43048914C>G | GRCh37 |
| NC_000008.9:g.43168071C>G | NCBI36 |
| NG_009552.1:g.58323C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379644.9:c.1392C>G MANE Select | ENSP00000368965.4:p.Thr464= | |
| ENST00000379644.8:c.1392C>G | ENSP00000368965.4:p.Thr464= | |
| ENST00000520678.1:n.325C>G | ||
| ENST00000521576.1:c.543C>G | ENSP00000429029.1:p.Thr181= | |
| ENST00000524016.5:c.496C>G | ||
| NM_152419.2:c.1392C>G | NP_689632.2:p.Thr464= | |
| XM_005273409.1:c.1392C>G | XP_005273466.1:p.Thr464= | |
| XM_005273410.1:c.1392C>G | XP_005273467.1:p.Thr464= | |
| XM_005273411.1:c.1200C>G | XP_005273468.1:p.Thr400= | |
| XM_005273412.2:c.1392C>G | XP_005273469.1:p.Thr464= | |
| NM_001363227.1:c.1392C>G | NP_001350156.1:p.Thr464= | |
| NM_001363228.1:c.1200C>G | NP_001350157.1:p.Thr400= | |
| NM_001363229.1:c.528C>G | NP_001350158.1:p.Thr176= | |
| XM_005273412.4:c.1392C>G | XP_005273469.1:p.Thr464= | |
| NM_152419.3:c.1392C>G MANE Select | NP_689632.2:p.Thr464= | |
| NM_001363227.2:c.1392C>G | NP_001350156.1:p.Thr464= | |
| NM_001363228.2:c.1200C>G | NP_001350157.1:p.Thr400= | |
| NM_001363229.2:c.528C>G | NP_001350158.1:p.Thr176= |