HGVS | Genome Assembly |
---|---|
NC_000004.12:g.38813881A>C , CM000666.2:g.38813881A>C | GRCh38 |
NC_000004.11:g.38815502A>C , CM000666.1:g.38815502A>C | GRCh37 |
NC_000004.10:g.38491897A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000506146.5:c.-352-8688T>G | ENSP00000423725.1:n.-352-8688T>G |