HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2444696C= , CM000673.2:g.2444696C= | GRCh38 |
NC_000011.9:g.2465926C= , CM000673.1:g.2465926C= | GRCh37 |
NC_000011.8:g.2422502C= | NCBI36 |
NG_008935.1:g.4706C= , LRG_287:g.4706C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000496887.7:c.11C= | ENSP00000434560.2:p.Ala4= | |
ENST00000496887.6:c.11C= | ENSP00000434560.1:p.Ala4= |