HGVS | Genome Assembly |
---|---|
NC_000010.11:g.122454933C>G , CM000672.2:g.122454933C>G | GRCh38 |
NC_000010.10:g.124214449C>G , CM000672.1:g.124214449C>G | GRCh37 |
NC_000010.9:g.124204439C>G | NCBI36 |
NG_011725.1:g.5271C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000528446.1:c.206C>G MANE Select | ENSP00000436682.1:p.Ala69Gly | |
NM_001099667.1:c.206C>G | NP_001093137.1:p.Ala69Gly | |
XR_946382.1:n.1827+3562G>C | ||
XR_946383.1:n.1827+3562G>C | ||
XR_946384.1:n.1576+3562G>C | ||
NM_001099667.2:c.206C>G | NP_001093137.1:p.Ala69Gly | |
XR_946382.2:n.1855+3562G>C | ||
XR_946383.2:n.1855+3562G>C | ||
XR_946384.2:n.1580+3562G>C | ||
NM_001099667.3:c.206C>G MANE Select | NP_001093137.1:p.Ala69Gly |