Linked Data
dbSNP Id:
rs1196477073
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8771594G>A , CM000665.2:g.8771594G>A | GRCh38 |
| NC_000003.11:g.8813280G>A , CM000665.1:g.8813280G>A | GRCh37 |
| NC_000003.10:g.8788280G>A | NCBI36 |
| NG_008797.2:g.42785G>A , LRG_329:g.42785G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000472766.1:n.156-5883G>A (CAV3) | ||
| XM_011533763.1:c.-238-3003C>T (OXTR) | XP_011532065.1:n.-238-3003C>T |