HGVS | Genome Assembly |
---|---|
NC_000013.11:g.110169535_110169536del , CM000675.2:g.110169535_110169536del | GRCh38 |
NC_000013.10:g.110821882_110821883del , CM000675.1:g.110821882_110821883del | GRCh37 |
NC_000013.9:g.109619883_109619884del | NCBI36 |
NG_011544.2:g.142615_142616del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375820.10:c.3876+94_3876+95del MANE Select | ENSP00000364979.4:n.3876+94_3876+95del | |
ENST00000650424.1:c.32+94_32+95del | ||
ENST00000375820.8:c.3876+94_3876+95del | ENSP00000364979.4:n.3876+94_3876+95del | |
NM_001845.5:c.3876+94_3876+95del | NP_001836.3:n.3876+94_3876+95del | |
XM_011521048.1:c.3684+94_3684+95del | XP_011519350.1:n.3684+94_3684+95del | |
XM_011521048.2:c.3684+94_3684+95del | XP_011519350.1:n.3684+94_3684+95del | |
NM_001845.6:c.3876+94_3876+95del MANE Select | NP_001836.3:n.3876+94_3876+95del |