HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99792608G>C , CM000666.2:g.99792608G>C | GRCh38 |
NC_000004.11:g.100713765G>C , CM000666.1:g.100713765G>C | GRCh37 |
NC_000004.10:g.100932788G>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
XM_006714431.1:c.-32+29035C>G | XP_006714494.1:n.-32+29035C>G |