Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8771452C>T , CM000665.2:g.8771452C>T | GRCh38 |
| NC_000003.11:g.8813138C>T , CM000665.1:g.8813138C>T | GRCh37 |
| NC_000003.10:g.8788138C>T | NCBI36 |
| NG_008797.2:g.42643C>T , LRG_329:g.42643C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000472766.1:n.156-6025C>T (CAV3) | ||
| XM_011533763.1:c.-238-2861G>A (OXTR) | XP_011532065.1:n.-238-2861G>A |