HGVS | Genome Assembly |
---|---|
NC_000024.10:g.19579903C>T , CM000686.2:g.19579903C>T | GRCh38 |
NC_000024.9:g.21741789C>T , CM000686.1:g.21741789C>T | GRCh37 |
NC_000024.8:g.20201177C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000686158.1:n.200-7307C>T | ||
ENST00000686905.1:n.134-7307C>T | ||
ENST00000693214.1:n.222-7307C>T | ||
ENST00000445715.6:n.102-7307C>T | ||
ENST00000407724.7:n.171-7307C>T | ||
ENST00000445715.5:n.102-7307C>T | ||
ENST00000447202.2:n.124-7307C>T | ||
ENST00000447520.5:n.102-7307C>T | ||
ENST00000459719.6:n.222-7307C>T | ||
ENST00000538014.2:n.241-7307C>T | ||
NR_045128.1:n.126-7307C>T | ||
NR_045129.1:n.126-7307C>T |