Canonical Allele Identifier:
CA106483435
Gene:
MyVariant.info:
GRCh38
chr4:g.130729712G>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.130729712G>T , CM000666.2:g.130729712G>T | GRCh38 |
| NC_000004.11:g.131650867G>T , CM000666.1:g.131650867G>T | GRCh37 |
| NC_000004.10:g.131870317G>T | NCBI36 |