Linked Data
ClinVar Variation Id:
1707166
dbSNP Id:
rs1311535007
gnomAD v2:
10-50678723-G-C
gnomAD v4:
10-49470677-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.49470677G>C , CM000672.2:g.49470677G>C | GRCh38 |
| NC_000010.10:g.50678723G>C , CM000672.1:g.50678723G>C | GRCh37 |
| NC_000010.9:g.50348729G>C | NCBI36 |
| NG_009442.1:g.73425C>G , LRG_465:g.73425C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355832.10:c.3283C>G MANE Select | ENSP00000348089.5:p.Pro1095Ala | |
| ENST00000679552.1:n.354C>G | ||
| ENST00000679871.1:n.429C>G | ||
| ENST00000679974.1:n.332C>G | ||
| ENST00000681632.1:n.4686C>G | ||
| ENST00000681659.1:c.3124C>G | ENSP00000505631.1:p.Pro1042Ala | |
| ENST00000355832.9:c.3283C>G | ENSP00000348089.5:p.Pro1095Ala | |
| ENST00000623073.3:c.*1579C>G | ENSP00000485650.1:n.*1579C>G | |
| ENST00000623115.3:c.1393C>G | ENSP00000485321.1:p.Pro465Ala | |
| ENST00000624341.3:c.1115C>G | ||
| NM_000124.3:c.3283C>G | NP_000115.1:p.Pro1095Ala | |
| XR_945953.1:n.243-888G>C | ||
| NM_001346440.1:c.3283C>G | NP_001333369.1:p.Pro1095Ala | |
| NM_000124.4:c.3283C>G MANE Select | NP_000115.1:p.Pro1095Ala | |
| NM_001346440.2:c.3283C>G | NP_001333369.1:p.Pro1095Ala |