HGVS | Genome Assembly |
---|---|
NC_000021.9:g.33026378G= , CM000683.2:g.33026378G= | GRCh38 |
NC_000021.8:g.34398686G= , CM000683.1:g.34398686G= | GRCh37 |
NC_000021.7:g.33320556G= | NCBI36 |
NG_011834.1:g.5448G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000382357.4:c.-63+352G= MANE Select | ENSP00000371794.3:n.-63+352G= | |
ENST00000333337.3:c.-485G= | ENSP00000331040.3:n.-485G= | |
ENST00000382357.3:c.-63+352G= | ENSP00000371794.3:n.-63+352G= | |
ENST00000430860.1:c.-63+118G= | ENSP00000391183.1:n.-63+118G= | |
NM_005806.3:c.-63+352G= | NP_005797.1:n.-63+352G= | |
XM_005260908.1:c.-63+118G= | XP_005260965.1:n.-63+118G= | |
NM_005806.4:c.-63+352G= MANE Select | NP_005797.1:n.-63+352G= |