HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149570269_149570271del , CM000664.2:g.149570269_149570271del | GRCh38 |
NC_000002.11:g.150426783_150426785del , CM000664.1:g.150426783_150426785del | GRCh37 |
NC_000002.10:g.150135029_150135031del | NCBI36 |
NG_009189.1:g.22546_22548del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.697-103_697-101del MANE Select | ENSP00000301920.5:n.697-103_697-101del | |
ENST00000303319.9:c.697-103_697-101del | ENSP00000301920.5:n.697-103_697-101del | |
ENST00000422782.2:c.799-103_799-101del | ENSP00000408331.2:n.799-103_799-101del | |
ENST00000428879.5:c.697-103_697-101del | ENSP00000389060.1:n.697-103_697-101del | |
NM_015702.2:c.697-103_697-101del | NP_056517.1:n.697-103_697-101del | |
NM_015702.3:c.697-103_697-101del MANE Select | NP_056517.1:n.697-103_697-101del |