HGVS | Genome Assembly |
---|---|
NC_000022.11:g.42132692T= , CM000684.2:g.42132692T= | GRCh38 |
NC_000022.10:g.42528699T= , CM000684.1:g.42528699T= | GRCh37 |
NC_000022.9:g.40858643T= | NCBI36 |
NG_008376.3:g.2300A= | |
NG_008376.4:g.3119A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000417586.1:n.150T= | ||
XM_011529967.1:c.-1045-856A= | XP_011528269.1:n.-1045-856A= |