HGVS | Genome Assembly |
---|---|
NC_000014.9:g.96204908C>G , CM000676.2:g.96204908C>G | GRCh38 |
NC_000014.8:g.96671245C>G , CM000676.1:g.96671245C>G | GRCh37 |
NC_000014.7:g.95740998C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000554311.2:c.-91C>G MANE Select | ENSP00000450482.1:n.-91C>G | |
ENST00000539359.1:c.-333C>G | ENSP00000438376.1:n.-333C>G | |
ENST00000542454.2:c.-2859C>G | ENSP00000439459.2:n.-2859C>G | |
ENST00000553811.1:c.-86C>G | ENSP00000450984.1:n.-86C>G | |
ENST00000554311.1:c.-91C>G | ENSP00000450482.1:n.-91C>G | |
NM_000623.3:c.-86C>G | NP_000614.1:n.-86C>G | |
NM_000623.4:c.-86C>G | NP_000614.1:n.-86C>G | |
NM_001379692.1:c.-91C>G MANE Select | NP_001366621.1:n.-91C>G |