HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94941791T>C , CM000672.2:g.94941791T>C | GRCh38 |
NC_000010.10:g.96701548T>C , CM000672.1:g.96701548T>C | GRCh37 |
NC_000010.9:g.96691538T>C | NCBI36 |
NG_008385.1:g.8134T>C | |
NG_008385.2:g.8634T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260682.8:c.169-67T>C MANE Select | ENSP00000260682.6:n.169-67T>C | |
ENST00000643112.1:c.169-67T>C | ENSP00000496202.1:n.169-67T>C | |
ENST00000645207.1:n.255T>C | ||
ENST00000260682.6:c.169-67T>C | ENSP00000260682.6:n.169-67T>C | |
ENST00000461906.1:n.194-67T>C | ||
NM_000771.3:c.169-67T>C | NP_000762.2:n.169-67T>C | |
NM_000771.4:c.169-67T>C MANE Select | NP_000762.2:n.169-67T>C |