HGVS | Genome Assembly |
---|---|
NC_000021.9:g.33026413T= , CM000683.2:g.33026413T= | GRCh38 |
NC_000021.8:g.34398721T= , CM000683.1:g.34398721T= | GRCh37 |
NC_000021.7:g.33320591T= | NCBI36 |
NG_011834.1:g.5483T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000382357.4:c.-62-388T= MANE Select | ENSP00000371794.3:n.-62-388T= | |
ENST00000333337.3:c.-450T= | ENSP00000331040.3:n.-450T= | |
ENST00000382357.3:c.-62-388T= | ENSP00000371794.3:n.-62-388T= | |
ENST00000430860.1:c.-63+153T= | ENSP00000391183.1:n.-63+153T= | |
NM_005806.3:c.-62-388T= | NP_005797.1:n.-62-388T= | |
XM_005260908.1:c.-63+153T= | XP_005260965.1:n.-63+153T= | |
NM_005806.4:c.-62-388T= MANE Select | NP_005797.1:n.-62-388T= |