Canonical Allele Identifier:
CA249552684
Gene:
MyVariant.info:
GRCh38
chr13:g.44234038C>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.44234038C>G , CM000675.2:g.44234038C>G | GRCh38 |
| NC_000013.10:g.44808174C>G , CM000675.1:g.44808174C>G | GRCh37 |
| NC_000013.9:g.43706174C>G | NCBI36 |