Linked Data
ClinVar Variation Id:
2139429
ClinVar RCV Id:
RCV003070824
gnomAD v4:
9-35657942-G-C
MyVariant Identifiers:
chr9:g.35657939G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.35657942G>C , CM000671.2:g.35657942G>C | GRCh38 |
| NC_000009.11:g.35657939G>C , CM000671.1:g.35657939G>C | GRCh37 |
| NC_000009.10:g.35647939G>C | NCBI36 |
| NG_017041.1:g.5077C>G , LRG_163:g.5077C>G | |
| NG_033120.1:g.4653G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003051.3:n.77C>G , LRG_163t1:n.77C>G |