HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663464C>A , CM000676.2:g.36663464C>A | GRCh38 |
NC_000014.8:g.37132669C>A , CM000676.1:g.37132669C>A | GRCh37 |
NC_000014.7:g.36202420C>A | NCBI36 |
NG_013357.1:g.10897C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000361487.7:c.572C>A MANE Select | ENSP00000355245.6:p.Thr191Asn | |
ENST00000361487.6:c.572C>A | ENSP00000355245.6:p.Thr191Asn | |
ENST00000402703.6:c.572C>A | ENSP00000384817.2:p.Thr191Asn | |
ENST00000554201.1:c.11C>A | ENSP00000450434.1:p.Thr4Asn | |
NM_006194.3:c.572C>A | NP_006185.1:p.Thr191Asn | |
NM_001372076.1:c.572C>A MANE Select | NP_001359005.1:p.Thr191Asn | |
NM_006194.4:c.572C>A | NP_006185.1:p.Thr191Asn |