Linked Data
ClinVar Variation Id:
351845
dbSNP Id:
rs563916447
gnomAD v2:
5-148381216-T-C
gnomAD v3:
5-149001653-T-C
gnomAD v4:
5-149001653-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149001653T>C , CM000667.2:g.149001653T>C | GRCh38 |
| NC_000005.9:g.148381216T>C , CM000667.1:g.148381216T>C | GRCh37 |
| NC_000005.8:g.148361409T>C | NCBI36 |
| NG_007947.2:g.66522A>G , LRG_269:g.66522A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000515425.6:c.*3058A>G MANE Select | ENSP00000423660.1:n.*3058A>G | |
| ENST00000643113.1:c.1700A>G | ||
| ENST00000675793.1:c.*7982A>G | ENSP00000502039.1:n.*7982A>G | |
| ENST00000323829.9:c.*6313A>G | ENSP00000313025.5:n.*6313A>G | |
| ENST00000504690.5:c.*12+2073A>G | ENSP00000425627.1:n.*12+2073A>G | |
| ENST00000510350.1:n.231+5228A>G | ||
| NM_024577.3:c.*3058A>G , LRG_269t1:c.*3058A>G | NP_078853.2:n.*3058A>G | |
| NM_024577.4:c.*3058A>G MANE Select | NP_078853.2:n.*3058A>G |