Linked Data
dbSNP Id:
rs112724034
gnomAD v4:
5-109885325-C-A
MyVariant Identifiers:
chr5:g.109221026C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.109885325C>A , CM000667.2:g.109885325C>A | GRCh38 |
| NC_000005.9:g.109221026C>A , CM000667.1:g.109221026C>A | GRCh37 |
| NC_000005.8:g.109248925C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000518923.1:n.99G>T (PGAM5P1) | ||
| NR_033175.1:n.1092C>A (LINC01848) |