HGVS | Genome Assembly |
---|---|
NC_000016.10:g.4951201T>A , CM000678.2:g.4951201T>A | GRCh38 |
NC_000016.9:g.5001202T>A , CM000678.1:g.5001202T>A | GRCh37 |
NC_000016.8:g.4941203T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000592772.1:c.-92+9363A>T | ENSP00000467699.1:n.-92+9363A>T |