HGVS | Genome Assembly |
---|---|
NC_000014.9:g.96204803T>G , CM000676.2:g.96204803T>G | GRCh38 |
NC_000014.8:g.96671140T>G , CM000676.1:g.96671140T>G | GRCh37 |
NC_000014.7:g.95740893T>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000542454.2:c.-2964T>G | ENSP00000439459.2:n.-2964T>G | |
ENST00000554311.1:c.-196T>G | ENSP00000450482.1:n.-196T>G | |
NM_000623.3:c.-191T>G | NP_000614.1:n.-191T>G |