Linked Data
ClinVar Variation Id:
437823
ClinVar RCV Id:
RCV000502628
dbSNP Id:
rs751716397
ExAC:
6:99322150 T / C
gnomAD v2:
6-99322150-T-C
gnomAD v4:
6-98874274-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98874274T>C , CM000668.2:g.98874274T>C | GRCh38 |
| NC_000006.11:g.99322150T>C , CM000668.1:g.99322150T>C | GRCh37 |
| NC_000006.10:g.99428871T>C | NCBI36 |
| NG_033903.1:g.78733A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369244.7:c.*4A>G MANE Select | ENSP00000358247.1:n.*4A>G | |
| ENST00000229971.2:c.*4A>G | ENSP00000229971.1:n.*4A>G | |
| ENST00000369244.6:c.*4A>G | ENSP00000358247.1:n.*4A>G | |
| NM_001278716.1:c.*4A>G | NP_001265645.1:n.*4A>G | |
| NM_012160.4:c.*4A>G | NP_036292.2:n.*4A>G | |
| NR_103836.1:n.1915A>G | ||
| XM_005266930.1:c.*4A>G | XP_005266987.1:n.*4A>G | |
| XM_005266930.3:c.*4A>G | XP_005266987.1:n.*4A>G | |
| XM_017010726.1:c.*4A>G | XP_016866215.1:n.*4A>G | |
| XM_017010727.2:c.*4A>G | XP_016866216.1:n.*4A>G | |
| XM_017010728.1:c.*4A>G | XP_016866217.1:n.*4A>G | |
| NM_001278716.2:c.*4A>G MANE Select | NP_001265645.1:n.*4A>G | |
| NR_103836.2:n.1855A>G | ||
| NM_012160.5:c.*4A>G | NP_036292.2:n.*4A>G |