Canonical Allele Identifier:
CA422484896
Gene:
Linked Data
dbSNP Id:
rs1665423030
gnomAD v4:
1-192800695-G-A
MyVariant Identifiers:
chr1:g.192769825G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.192800695G>A , CM000663.2:g.192800695G>A | GRCh38 |
| NC_000001.10:g.192769825G>A , CM000663.1:g.192769825G>A | GRCh37 |
| NC_000001.9:g.191036448G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429211.2:n.125G>A |