HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780553G= , CM000672.2:g.94780553G= | GRCh38 |
NC_000010.10:g.96540310G= , CM000672.1:g.96540310G= | GRCh37 |
NC_000010.9:g.96530300G= | NCBI36 |
NG_008384.2:g.22848G= | |
NG_008384.3:g.22873G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371321.9:c.536G= MANE Select | ENSP00000360372.3:p.Cys179= | |
ENST00000645461.1:n.1589G= | ||
ENST00000371321.7:c.536G= | ENSP00000360372.3:p.Cys179= | |
ENST00000464755.1:c.1299G= | ENSP00000483243.1:n.1299G= | |
NM_000769.2:c.536G= | NP_000760.1:p.Cys179= | |
NM_000769.4:c.536G= MANE Select | NP_000760.1:p.Cys179= |