HGVS | Genome Assembly |
---|---|
NC_000005.10:g.157110425C>T , CM000667.2:g.157110425C>T | GRCh38 |
NC_000005.9:g.156537436C>T , CM000667.1:g.156537436C>T | GRCh37 |
NC_000005.8:g.156470014C>T | NCBI36 |
NG_030444.1:g.3813G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000524219.2:c.-293-3463G>A | ENSP00000430328.2:n.-293-3463G>A | |
ENST00000696899.1:c.-264-1178G>A | ENSP00000512960.1:n.-264-1178G>A | |
ENST00000524219.1:c.-293-3463G>A | ENSP00000430328.1:n.-293-3463G>A |