HGVS | Genome Assembly |
---|---|
NC_000012.12:g.10446008C>T , CM000674.2:g.10446008C>T | GRCh38 |
NC_000012.11:g.10598607C>T , CM000674.1:g.10598607C>T | GRCh37 |
NC_000012.10:g.10489874C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000536188.5:c.685+560G>A | ENSP00000441432.1:n.685+560G>A | |
NM_001304448.1:c.685+560G>A | NP_001291377.1:n.685+560G>A | |
XM_024448973.1:c.685+560G>A | XP_024304741.1:n.685+560G>A |