Linked Data
ClinVar Variation Id:
2153032
ClinVar RCV Id:
RCV003085457
dbSNP Id:
rs1647834881
gnomAD v4:
1-115732883-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.115732883G>A , CM000663.2:g.115732883G>A | GRCh38 |
| NC_000001.10:g.116275504G>A , CM000663.1:g.116275504G>A | GRCh37 |
| NC_000001.9:g.116077027G>A | NCBI36 |
| NG_008802.1:g.40923C>T , LRG_404:g.40923C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000488931.2:c.330+18C>T | ENSP00000518226.1:n.330+18C>T | |
| ENST00000261448.6:c.606+18C>T MANE Select | ENSP00000261448.5:n.606+18C>T | |
| ENST00000261448.5:c.606+18C>T | ENSP00000261448.5:n.606+18C>T | |
| ENST00000488931.1:n.27+18C>T | ||
| NM_001232.3:c.606+18C>T , LRG_404t1:c.606+18C>T | NP_001223.2:n.606+18C>T | |
| NM_001232.4:c.606+18C>T MANE Select | NP_001223.2:n.606+18C>T |