HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135031107A= , CM000667.2:g.135031107A= | GRCh38 |
NC_000005.9:g.134366797A= , CM000667.1:g.134366797A= | GRCh37 |
NC_000005.8:g.134394696A= | NCBI36 |
NG_012114.1:g.8168T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265340.12:c.402+169T= MANE Select | ENSP00000265340.6:n.402+169T= | |
ENST00000265340.11:c.402+169T= | ENSP00000265340.6:n.402+169T= | |
ENST00000503586.1:c.524+169T= | ||
ENST00000504936.1:n.735+169T= | ||
ENST00000506438.5:c.402+169T= | ENSP00000427542.1:n.402+169T= | |
NM_002653.4:c.402+169T= | NP_002644.4:n.402+169T= | |
NM_002653.5:c.402+169T= MANE Select | NP_002644.4:n.402+169T= |