HGVS | Genome Assembly |
---|---|
NC_000005.10:g.135031088G>A , CM000667.2:g.135031088G>A | GRCh38 |
NC_000005.9:g.134366778G>A , CM000667.1:g.134366778G>A | GRCh37 |
NC_000005.8:g.134394677G>A | NCBI36 |
NG_012114.1:g.8187C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265340.12:c.402+188C>T MANE Select | ENSP00000265340.6:n.402+188C>T | |
ENST00000265340.11:c.402+188C>T | ENSP00000265340.6:n.402+188C>T | |
ENST00000503586.1:c.524+188C>T | ||
ENST00000504936.1:n.735+188C>T | ||
ENST00000506438.5:c.402+188C>T | ENSP00000427542.1:n.402+188C>T | |
NM_002653.4:c.402+188C>T | NP_002644.4:n.402+188C>T | |
NM_002653.5:c.402+188C>T MANE Select | NP_002644.4:n.402+188C>T |