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