HGVS | Genome Assembly |
---|---|
NC_000021.9:g.33026415T= , CM000683.2:g.33026415T= | GRCh38 |
NC_000021.8:g.34398723T= , CM000683.1:g.34398723T= | GRCh37 |
NC_000021.7:g.33320593T= | NCBI36 |
NG_011834.1:g.5485T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000382357.4:c.-62-386T= MANE Select | ENSP00000371794.3:n.-62-386T= | |
ENST00000333337.3:c.-448T= | ENSP00000331040.3:n.-448T= | |
ENST00000382357.3:c.-62-386T= | ENSP00000371794.3:n.-62-386T= | |
ENST00000430860.1:c.-63+155T= | ENSP00000391183.1:n.-63+155T= | |
NM_005806.3:c.-62-386T= | NP_005797.1:n.-62-386T= | |
XM_005260908.1:c.-63+155T= | XP_005260965.1:n.-63+155T= | |
NM_005806.4:c.-62-386T= MANE Select | NP_005797.1:n.-62-386T= |