HGVS | Genome Assembly |
---|---|
NC_000002.12:g.149569870_149569873del , CM000664.2:g.149569870_149569873del | GRCh38 |
NC_000002.11:g.150426384_150426387del , CM000664.1:g.150426384_150426387del | GRCh37 |
NC_000002.10:g.150134630_150134633del | NCBI36 |
NG_009189.1:g.22949_22952del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303319.10:c.*106_*109del MANE Select | ENSP00000301920.5:n.*106_*109del | |
ENST00000303319.9:c.*106_*109del | ENSP00000301920.5:n.*106_*109del | |
ENST00000422782.2:c.*106_*109del | ENSP00000408331.2:n.*106_*109del | |
ENST00000428879.5:c.*106_*109del | ENSP00000389060.1:n.*106_*109del | |
NM_015702.2:c.*106_*109del | NP_056517.1:n.*106_*109del | |
NM_015702.3:c.*106_*109del MANE Select | NP_056517.1:n.*106_*109del |