HGVS | Genome Assembly |
---|---|
NC_000003.12:g.8772326T>C , CM000665.2:g.8772326T>C | GRCh38 |
NC_000003.11:g.8814012T>C , CM000665.1:g.8814012T>C | GRCh37 |
NC_000003.10:g.8789012T>C | NCBI36 |
NG_008797.2:g.43517T>C , LRG_329:g.43517T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000472766.1:n.156-5151T>C (CAV3) | ||
XM_011533763.1:c.-238-3735A>G (OXTR) | XP_011532065.1:n.-238-3735A>G |