HGVS | Genome Assembly |
---|---|
NC_000022.11:g.27750794_27750796del , CM000684.2:g.27750794_27750796del | GRCh38 |
NC_000022.10:g.28146782_28146784del , CM000684.1:g.28146782_28146784del | GRCh37 |
NC_000022.9:g.26476782_26476784del | NCBI36 |
NG_023258.1:g.55703_55705del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703102.1:n.607_609del | ||
ENST00000302326.5:c.*119_*121del MANE Select | ENSP00000304956.4:n.*119_*121del | |
ENST00000302326.4:c.*119_*121del | ENSP00000304956.4:n.*119_*121del | |
ENST00000424656.1:c.435_437del | ||
ENST00000497225.1:n.438_440del | ||
NM_002430.2:c.*119_*121del | NP_002421.3:n.*119_*121del | |
NM_002430.3:c.*119_*121del MANE Select | NP_002421.3:n.*119_*121del |