HGVS | Genome Assembly |
---|---|
NC_000014.9:g.96204868A>T , CM000676.2:g.96204868A>T | GRCh38 |
NC_000014.8:g.96671205A>T , CM000676.1:g.96671205A>T | GRCh37 |
NC_000014.7:g.95740958A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000554311.2:c.-131A>T MANE Select | ENSP00000450482.1:n.-131A>T | |
ENST00000539359.1:c.-373A>T | ENSP00000438376.1:n.-373A>T | |
ENST00000542454.2:c.-2899A>T | ENSP00000439459.2:n.-2899A>T | |
ENST00000553811.1:c.-126A>T | ENSP00000450984.1:n.-126A>T | |
ENST00000554311.1:c.-131A>T | ENSP00000450482.1:n.-131A>T | |
NM_000623.3:c.-126A>T | NP_000614.1:n.-126A>T | |
NM_000623.4:c.-126A>T | NP_000614.1:n.-126A>T | |
NM_001379692.1:c.-131A>T MANE Select | NP_001366621.1:n.-131A>T |