HGVS | Genome Assembly |
---|---|
NC_000008.11:g.63038906C>A , CM000670.2:g.63038906C>A | GRCh38 |
NC_000008.10:g.63951465C>A , CM000670.1:g.63951465C>A | GRCh37 |
NC_000008.9:g.64114019C>A | NCBI36 |
NG_028126.1:g.5146G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000677327.1:n.502G>T | ||
ENST00000679326.1:c.-138G>T | ENSP00000504262.1:n.-138G>T | |
ENST00000260118.6:c.-138G>T | ENSP00000260118.6:n.-138G>T | |
NM_003878.2:c.-138G>T | NP_003869.1:n.-138G>T | |
XM_011517623.1:c.-138G>T | XP_011515925.1:n.-138G>T |