HGVS | Genome Assembly |
---|---|
NC_000002.12:g.184913696_184913697del , CM000664.2:g.184913696_184913697del | GRCh38 |
NC_000002.11:g.185778423_185778424del , CM000664.1:g.185778423_185778424del | GRCh37 |
NC_000002.10:g.185486668_185486669del | NCBI36 |
NG_046950.1:g.320331_320332del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000302277.7:c.256-19907_256-19906del MANE Select | ENSP00000303252.6:n.256-19907_256-19906del | |
ENST00000302277.6:c.256-19907_256-19906del | ENSP00000303252.6:n.256-19907_256-19906del | |
ENST00000613975.1:c.1-19907_1-19906del | ENSP00000483032.1:n.1-19907_1-19906del | |
NM_194250.1:c.256-19907_256-19906del | NP_919226.1:n.256-19907_256-19906del | |
NM_194250.2:c.256-19907_256-19906del MANE Select | NP_919226.1:n.256-19907_256-19906del |