HGVS | Genome Assembly |
---|---|
NC_000010.11:g.70441602C>A , CM000672.2:g.70441602C>A | GRCh38 |
NC_000010.10:g.72201358C>A , CM000672.1:g.72201358C>A | GRCh37 |
NC_000010.9:g.71871364C>A | NCBI36 |
NG_012448.1:g.5108G>T | |
NG_012448.2:g.11347G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000287139.8:c.66G>T MANE Select | ENSP00000287139.3:p.Ala22= | |
ENST00000287139.7:c.66G>T | ENSP00000287139.3:p.Ala22= | |
ENST00000414871.1:c.29-5619G>T | ENSP00000394468.1:n.29-5619G>T | |
NM_018055.4:c.66G>T | NP_060525.3:p.Ala22= | |
NM_001329906.1:c.-206-5619G>T | NP_001316835.1:n.-206-5619G>T | |
XM_024448028.1:c.-207+429G>T | XP_024303796.1:n.-207+429G>T | |
NM_018055.5:c.66G>T MANE Select | NP_060525.3:p.Ala22= | |
NM_001329906.2:c.-206-5619G>T | NP_001316835.1:n.-206-5619G>T |