HGVS | Genome Assembly |
---|---|
NC_000003.12:g.8771556T>A , CM000665.2:g.8771556T>A | GRCh38 |
NC_000003.11:g.8813242T>A , CM000665.1:g.8813242T>A | GRCh37 |
NC_000003.10:g.8788242T>A | NCBI36 |
NG_008797.2:g.42747T>A , LRG_329:g.42747T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000472766.1:n.156-5921T>A (CAV3) | ||
XM_011533763.1:c.-238-2965A>T (OXTR) | XP_011532065.1:n.-238-2965A>T |