HGVS | Genome Assembly |
---|---|
NC_000012.12:g.10445973T>C , CM000674.2:g.10445973T>C | GRCh38 |
NC_000012.11:g.10598572T>C , CM000674.1:g.10598572T>C | GRCh37 |
NC_000012.10:g.10489839T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000536188.5:c.685+595A>G | ENSP00000441432.1:n.685+595A>G | |
NM_001304448.1:c.685+595A>G | NP_001291377.1:n.685+595A>G | |
XM_024448973.1:c.685+595A>G | XP_024304741.1:n.685+595A>G |