Linked Data
dbSNP Id:
rs1708754393
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8771566T>C , CM000665.2:g.8771566T>C | GRCh38 |
| NC_000003.11:g.8813252T>C , CM000665.1:g.8813252T>C | GRCh37 |
| NC_000003.10:g.8788252T>C | NCBI36 |
| NG_008797.2:g.42757T>C , LRG_329:g.42757T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000472766.1:n.156-5911T>C (CAV3) | ||
| XM_011533763.1:c.-238-2975A>G (OXTR) | XP_011532065.1:n.-238-2975A>G |