HGVS | Genome Assembly |
---|---|
NC_000017.11:g.33066726G>T , CM000679.2:g.33066726G>T | GRCh38 |
NC_000017.10:g.31393744G>T , CM000679.1:g.31393744G>T | GRCh37 |
NC_000017.9:g.28417857G>T | NCBI36 |
NG_029763.1:g.1095082C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000225823.7:c.987+22137C>A MANE Select | ENSP00000225823.2:n.987+22137C>A | |
ENST00000225823.6:c.987+22137C>A | ENSP00000225823.2:n.987+22137C>A | |
ENST00000359872.6:c.834+22137C>A | ENSP00000352934.6:n.834+22137C>A | |
ENST00000448983.1:n.392+22137C>A | ||
NM_001094.4:c.834+22137C>A | NP_001085.2:n.834+22137C>A | |
NM_183377.1:c.987+22137C>A | NP_899233.1:n.987+22137C>A | |
NM_001094.5:c.834+22137C>A | NP_001085.2:n.834+22137C>A | |
NM_183377.2:c.987+22137C>A MANE Select | NP_899233.1:n.987+22137C>A |