HGVS | Genome Assembly |
---|---|
NC_000008.11:g.63038774T= , CM000670.2:g.63038774T= | GRCh38 |
NC_000008.10:g.63951333T= , CM000670.1:g.63951333T= | GRCh37 |
NC_000008.9:g.64113887T= | NCBI36 |
NG_028126.1:g.5278A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260118.7:c.-6A= MANE Select | ENSP00000260118.6:n.-6A= | |
ENST00000518113.2:c.-6A= | ENSP00000504520.1:n.-6A= | |
ENST00000523788.2:n.22A= | ||
ENST00000677327.1:n.634A= | ||
ENST00000677459.1:c.-6A= | ENSP00000503731.1:n.-6A= | |
ENST00000677482.1:c.-6A= | ENSP00000504590.1:n.-6A= | |
ENST00000678069.1:n.29A= | ||
ENST00000679326.1:c.-6A= | ENSP00000504262.1:n.-6A= | |
ENST00000260118.6:c.-6A= | ENSP00000260118.6:n.-6A= | |
ENST00000518966.5:n.28A= | ||
ENST00000520609.5:n.28A= | ||
ENST00000523788.1:n.29A= | ||
NM_003878.2:c.-6A= | NP_003869.1:n.-6A= | |
XM_011517623.1:c.-6A= | XP_011515925.1:n.-6A= | |
XM_011517623.3:c.-6A= | XP_011515925.1:n.-6A= | |
NM_003878.3:c.-6A= MANE Select | NP_003869.1:n.-6A= |