HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52038429T= , CM000666.2:g.52038429T= | GRCh38 |
NC_000004.11:g.52904595T= , CM000666.1:g.52904595T= | GRCh37 |
NC_000004.10:g.52599352T= | NCBI36 |
NG_008891.1:g.4891A= , LRG_204:g.4891A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000381431.9:c.-170A= | ENSP00000370839.5:n.-170A= |