HGVS | Genome Assembly |
---|---|
NC_000008.11:g.10494798C>A , CM000670.2:g.10494798C>A | GRCh38 |
NC_000008.10:g.10352308C>A , CM000670.1:g.10352308C>A | GRCh37 |
NC_000008.9:g.10389718C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000523024.2:c.343+2914G>T | ENSP00000518528.1:n.343+2914G>T | |
ENST00000521149.2:n.203+3930G>T | ||
ENST00000523024.1:n.609+2914G>T |