Linked Data
ClinVar Variation Id:
923104
ClinVar RCV Id:
RCV001183583
dbSNP Id:
rs17249141
gnomAD v4:
19-11089332-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11089332C>G , CM000681.2:g.11089332C>G | GRCh38 |
| NC_000019.9:g.11200008C>G , CM000681.1:g.11200008C>G | GRCh37 |
| NC_000019.8:g.11061008C>G | NCBI36 |
| NG_009060.1:g.4952C>G , LRG_274:g.4952C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_163945.1:n.328G>C |