HGVS | Genome Assembly |
---|---|
NC_000008.11:g.63038907C= , CM000670.2:g.63038907C= | GRCh38 |
NC_000008.10:g.63951466C= , CM000670.1:g.63951466C= | GRCh37 |
NC_000008.9:g.64114020C= | NCBI36 |
NG_028126.1:g.5145G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000677327.1:n.501G= | ||
ENST00000679326.1:c.-139G= | ENSP00000504262.1:n.-139G= | |
ENST00000260118.6:c.-139G= | ENSP00000260118.6:n.-139G= | |
NM_003878.2:c.-139G= | NP_003869.1:n.-139G= | |
XM_011517623.1:c.-139G= | XP_011515925.1:n.-139G= |