HGVS | Genome Assembly |
---|---|
NC_000021.9:g.33026382G>A , CM000683.2:g.33026382G>A | GRCh38 |
NC_000021.8:g.34398690G>A , CM000683.1:g.34398690G>A | GRCh37 |
NC_000021.7:g.33320560G>A | NCBI36 |
NG_011834.1:g.5452G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000382357.4:c.-63+356G>A MANE Select | ENSP00000371794.3:n.-63+356G>A | |
ENST00000333337.3:c.-481G>A | ENSP00000331040.3:n.-481G>A | |
ENST00000382357.3:c.-63+356G>A | ENSP00000371794.3:n.-63+356G>A | |
ENST00000430860.1:c.-63+122G>A | ENSP00000391183.1:n.-63+122G>A | |
NM_005806.3:c.-63+356G>A | NP_005797.1:n.-63+356G>A | |
XM_005260908.1:c.-63+122G>A | XP_005260965.1:n.-63+122G>A | |
NM_005806.4:c.-63+356G>A MANE Select | NP_005797.1:n.-63+356G>A |