Canonical Allele Identifier:
CA112973390
Gene:
MyVariant.info:
GRCh38
chr5:g.1447647G>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1447647G>T , CM000667.2:g.1447647G>T | GRCh38 |
| NC_000005.9:g.1447762G>T , CM000667.1:g.1447762G>T | GRCh37 |
| NC_000005.8:g.1500762G>T | NCBI36 |
| NG_015885.1:g.2782C>A |