HGVS | Genome Assembly |
---|---|
NC_000006.12:g.116882329_116882330del , CM000668.2:g.116882329_116882330del | GRCh38 |
NC_000006.11:g.117203492_117203493del , CM000668.1:g.117203492_117203493del | GRCh37 |
NC_000006.10:g.117310185_117310186del | NCBI36 |
NG_027699.1:g.10117_10118del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000332958.3:c.505-38_505-37del MANE Select | ENSP00000332208.2:n.505-38_505-37del | |
ENST00000332958.2:c.505-38_505-37del | ENSP00000332208.2:n.505-38_505-37del | |
ENST00000487683.5:n.569-38_569-37del | ||
NM_173560.3:c.505-38_505-37del | NP_775831.2:n.505-38_505-37del | |
XM_011535589.1:c.505-38_505-37del | XP_011533891.1:n.505-38_505-37del | |
XM_017010477.1:c.127-38_127-37del | XP_016865966.1:n.127-38_127-37del | |
NM_173560.4:c.505-38_505-37del MANE Select | NP_775831.2:n.505-38_505-37del |