Canonical Allele Identifier:
CA91734600
Gene:
Linked Data
dbSNP Id:
rs977814300
gnomAD v4:
4-5711166-C-T
MyVariant Identifiers:
chr4:g.5711166C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.5711166C>T , CM000666.2:g.5711166C>T | GRCh38 |
| NC_000004.11:g.5712893C>T , CM000666.1:g.5712893C>T | GRCh37 |
| NC_000004.10:g.5763794C>T | NCBI36 |
| NG_008843.1:g.4970C>T | |
| NG_015821.1:g.3383G>A |