HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15180615del , CM000681.2:g.15180615del | GRCh38 |
NC_000019.9:g.15291426del , CM000681.1:g.15291426del | GRCh37 |
NC_000019.8:g.15152426del | NCBI36 |
NG_009819.1:g.25367del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263388.7:c.3142+66del MANE Select | ENSP00000263388.1:n.3142+66del | |
ENST00000263388.6:c.3142+66del | ENSP00000263388.1:n.3142+66del | |
ENST00000601011.1:c.2983+66del | ENSP00000473138.1:n.2983+66del | |
NM_000435.2:c.3142+66del | NP_000426.2:n.3142+66del | |
XM_005259924.3:c.2986+66del | XP_005259981.1:n.2986+66del | |
XM_005259924.4:c.2986+66del | XP_005259981.1:n.2986+66del | |
NM_000435.3:c.3142+66del MANE Select | NP_000426.2:n.3142+66del |