HGVS | Genome Assembly |
---|---|
NC_000013.11:g.40644682_40644683del , CM000675.2:g.40644682_40644683del | GRCh38 |
NC_000013.10:g.41218819_41218820del , CM000675.1:g.41218819_41218820del | GRCh37 |
NC_000013.9:g.40116819_40116820del | NCBI36 |
NG_023244.1:g.26918_26919del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379561.6:c.630+20903_630+20904del MANE Select | ENSP00000368880.4:n.630+20903_630+20904del | |
ENST00000655267.1:n.333+20903_333+20904del | ||
ENST00000660760.1:n.296-11432_296-11431del | ||
ENST00000379561.5:c.630+20903_630+20904del | ENSP00000368880.4:n.630+20903_630+20904del | |
NM_002015.3:c.630+20903_630+20904del | NP_002006.2:n.630+20903_630+20904del | |
XR_941536.1:n.1226+659_1226+660del | ||
NM_002015.4:c.630+20903_630+20904del MANE Select | NP_002006.2:n.630+20903_630+20904del |