HGVS | Genome Assembly |
---|---|
NC_000008.11:g.1798784A>T , CM000670.2:g.1798784A>T | GRCh38 |
NC_000008.10:g.1746950A>T , CM000670.1:g.1746950A>T | GRCh37 |
NC_000008.9:g.1734357A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000635773.1:c.496+27187A>T | ||
ENST00000635855.1:c.543+27187A>T | ENSP00000489726.1:n.543+27187A>T | |
ENST00000636175.1:c.343+27187A>T | ||
ENST00000636934.1:c.544-1890A>T | ENSP00000490218.1:n.544-1890A>T |