HGVS | Genome Assembly |
---|---|
NC_000024.10:g.19577720C>A , CM000686.2:g.19577720C>A | GRCh38 |
NC_000024.9:g.21739606C>A , CM000686.1:g.21739606C>A | GRCh37 |
NC_000024.8:g.20198994C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000686158.1:n.200-9490C>A | ||
ENST00000686905.1:n.134-9490C>A | ||
ENST00000693214.1:n.222-9490C>A | ||
ENST00000445715.6:n.102-9490C>A | ||
ENST00000407724.7:n.171-9490C>A | ||
ENST00000445715.5:n.102-9490C>A | ||
ENST00000447202.2:n.124-9490C>A | ||
ENST00000447520.5:n.102-9490C>A | ||
ENST00000459719.6:n.222-9490C>A | ||
ENST00000538014.2:n.240+8261C>A | ||
NR_045128.1:n.126-9490C>A | ||
NR_045129.1:n.126-9490C>A |