HGVS | Genome Assembly |
---|---|
NC_000003.12:g.46208857T>C , CM000665.2:g.46208857T>C | GRCh38 |
NC_000003.11:g.46250348T>C , CM000665.1:g.46250348T>C | GRCh37 |
NC_000003.10:g.46225352T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000357422.2:c.-284-1834T>C | ENSP00000350003.2:n.-284-1834T>C |