HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91055356T>C , CM000674.2:g.91055356T>C | GRCh38 |
NC_000012.11:g.91449133T>C , CM000674.1:g.91449133T>C | GRCh37 |
NC_000012.10:g.89973264T>C | NCBI36 |
NG_021223.1:g.7999A>G , LRG_538:g.7999A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266719.4:c.886+40A>G MANE Select | ENSP00000266719.3:n.886+40A>G | |
ENST00000266719.3:c.886+40A>G | ENSP00000266719.3:n.886+40A>G | |
NM_007035.3:c.886+40A>G , LRG_538t1:c.886+40A>G | NP_008966.1:n.886+40A>G | |
XM_011537781.1:c.886+40A>G | XP_011536083.1:n.886+40A>G | |
NM_007035.4:c.886+40A>G MANE Select | NP_008966.1:n.886+40A>G |