HGVS | Genome Assembly |
---|---|
NC_000002.12:g.118079688A>C , CM000664.2:g.118079688A>C | GRCh38 |
NC_000002.11:g.118837264A>C , CM000664.1:g.118837264A>C | GRCh37 |
NC_000002.10:g.118553734A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_011512305.1:c.697-2156T>G | XP_011510607.1:n.697-2156T>G | |
XR_001739662.2:n.138+8563T>G |