Linked Data
ClinVar Variation Id:
1024266
ClinVar RCV Id:
RCV001324425
dbSNP Id:
rs775685036
gnomAD v3:
2-29070991-G-C
gnomAD v4:
2-29070991-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29070991G>C , CM000664.2:g.29070991G>C | GRCh38 |
| NC_000002.11:g.29293857G>C , CM000664.1:g.29293857G>C | GRCh37 |
| NC_000002.10:g.29147361G>C | NCBI36 |
| NG_021427.1:g.8271C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331664.6:c.3271C>G MANE Select | ENSP00000332809.4:p.Pro1091Ala | |
| ENST00000331664.5:c.3271C>G | ENSP00000332809.4:p.Pro1091Ala | |
| NM_001029883.2:c.3271C>G | NP_001025054.1:p.Pro1091Ala | |
| XM_011532826.1:c.3271C>G | XP_011531128.1:p.Pro1091Ala | |
| XR_939901.1:n.185+1824G>C | ||
| XR_939902.1:n.173+1836G>C | ||
| NM_001029883.3:c.3271C>G MANE Select | NP_001025054.1:p.Pro1091Ala |