Canonical Allele Identifier:
CA882068227
Gene:
MyVariant.info:
GRCh38
chr19:g.38645880C>T
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38645880C>T , CM000681.2:g.38645880C>T | GRCh38 |
| NC_000019.9:g.39136520C>T , CM000681.1:g.39136520C>T | GRCh37 |
| NC_000019.8:g.43828360C>T | NCBI36 |
| NG_007082.2:g.3194C>T |