HGVS | Genome Assembly |
---|---|
NC_000010.11:g.102821531A>C , CM000672.2:g.102821531A>C | GRCh38 |
NC_000010.10:g.104581288A>C , CM000672.1:g.104581288A>C | GRCh37 |
NC_000010.9:g.104571278A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647664.1:c.442+228A>C | ENSP00000498131.1:n.442+228A>C |