HGVS | Genome Assembly |
---|---|
NC_000021.9:g.33026153G>T , CM000683.2:g.33026153G>T | GRCh38 |
NC_000021.8:g.34398461G>T , CM000683.1:g.34398461G>T | GRCh37 |
NC_000021.7:g.33320331G>T | NCBI36 |
NG_011834.1:g.5223G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382357.4:c.-63+127G>T MANE Select | ENSP00000371794.3:n.-63+127G>T | |
ENST00000333337.3:c.-710G>T | ENSP00000331040.3:n.-710G>T | |
ENST00000382357.3:c.-63+127G>T | ENSP00000371794.3:n.-63+127G>T | |
ENST00000430860.1:c.-170G>T | ENSP00000391183.1:n.-170G>T | |
NM_005806.3:c.-63+127G>T | NP_005797.1:n.-63+127G>T | |
XM_005260908.1:c.-170G>T | XP_005260965.1:n.-170G>T | |
NM_005806.4:c.-63+127G>T MANE Select | NP_005797.1:n.-63+127G>T |