HGVS | Genome Assembly |
---|---|
NC_000010.11:g.14436553T>G , CM000672.2:g.14436553T>G | GRCh38 |
NC_000010.10:g.14478552T>G , CM000672.1:g.14478552T>G | GRCh37 |
NC_000010.9:g.14518558T>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000475141.2:c.-305+25515A>C | ENSP00000473870.1:n.-305+25515A>C | |
ENST00000493380.5:c.-82+25515A>C | ENSP00000474863.1:n.-82+25515A>C |