HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149570286_149570289del , CM000664.2:g.149570286_149570289del | GRCh38 |
NC_000002.11:g.150426800_150426803del , CM000664.1:g.150426800_150426803del | GRCh37 |
NC_000002.10:g.150135046_150135049del | NCBI36 |
NG_009189.1:g.22531_22534del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.697-118_697-115del MANE Select | ENSP00000301920.5:n.697-118_697-115del | |
ENST00000303319.9:c.697-118_697-115del | ENSP00000301920.5:n.697-118_697-115del | |
ENST00000422782.2:c.799-118_799-115del | ENSP00000408331.2:n.799-118_799-115del | |
ENST00000428879.5:c.697-118_697-115del | ENSP00000389060.1:n.697-118_697-115del | |
NM_015702.2:c.697-118_697-115del | NP_056517.1:n.697-118_697-115del | |
NM_015702.3:c.697-118_697-115del MANE Select | NP_056517.1:n.697-118_697-115del |