HGVS | Genome Assembly |
---|---|
NC_000004.12:g.89839677C>T , CM000666.2:g.89839677C>T | GRCh38 |
NC_000004.11:g.90760828C>T , CM000666.1:g.90760828C>T | GRCh37 |
NC_000004.10:g.90979851C>T | NCBI36 |
NG_011851.1:g.3620G>A |
HGVS | Amino-acid Change | |
---|---|---|
NR_045481.1:n.480+1271C>T |