HGVS | Genome Assembly |
---|---|
NC_000005.10:g.34008169T>A , CM000667.2:g.34008169T>A | GRCh38 |
NC_000005.9:g.34008274T>A , CM000667.1:g.34008274T>A | GRCh37 |
NC_000005.8:g.34044031T>A | NCBI36 |
NG_016211.1:g.4947A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382079.3:c.690-2270A>T | ENSP00000371511.3:n.690-2270A>T | |
NR_037951.1:n.765-2270A>T |