HGVS | Genome Assembly |
---|---|
NC_000011.10:g.14972978A>T , CM000673.2:g.14972978A>T | GRCh38 |
NC_000011.9:g.14994524A>T , CM000673.1:g.14994524A>T | GRCh37 |
NC_000011.8:g.14951100A>T | NCBI36 |
NG_015960.1:g.4309T>A , LRG_13:g.4309T>A |
HGVS | Amino-acid Change |
---|---|
ENST00000523376.5:c.-445-4913A>T | ENSP00000428882.1:n.-445-4913A>T |