HGVS | Genome Assembly |
---|---|
NC_000003.12:g.8771581T>C , CM000665.2:g.8771581T>C | GRCh38 |
NC_000003.11:g.8813267T>C , CM000665.1:g.8813267T>C | GRCh37 |
NC_000003.10:g.8788267T>C | NCBI36 |
NG_008797.2:g.42772T>C , LRG_329:g.42772T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000472766.1:n.156-5896T>C (CAV3) | ||
XM_011533763.1:c.-238-2990A>G (OXTR) | XP_011532065.1:n.-238-2990A>G |