HGVS | Genome Assembly |
---|---|
NC_000009.12:g.21140494C= , CM000671.2:g.21140494C= | GRCh38 |
NC_000009.11:g.21140493C= , CM000671.1:g.21140493C= | GRCh37 |
NC_000009.10:g.21130493C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380229.3:c.*489G= | ENSP00000369578.2:n.*489G= |