HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2445174_2445175del , CM000673.2:g.2445174_2445175del | GRCh38 |
NC_000011.9:g.2466404_2466405del , CM000673.1:g.2466404_2466405del | GRCh37 |
NC_000011.8:g.2422980_2422981del | NCBI36 |
NG_008935.1:g.5184_5185del , LRG_287:g.5184_5185del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000496887.7:c.24-209_24-208del | ENSP00000434560.2:n.24-209_24-208del | |
ENST00000646564.2:c.76_77del | ENSP00000495806.2:p.Gly26GlnfsTer? | |
ENST00000155840.12:c.76_77del MANE Select | ENSP00000155840.2:p.Gly26GlnfsTer? | |
ENST00000155840.9:c.76_77del | ENSP00000155840.2:p.Gly26GlnfsTer? | |
ENST00000496887.6:c.24-209_24-208del | ENSP00000434560.1:n.24-209_24-208del | |
NM_000218.2:c.76_77del , LRG_287t1:c.76_77del | NP_000209.2:p.Gly26GlnfsTer? | |
NM_000218.3:c.76_77del MANE Select | NP_000209.2:p.Gly26GlnfsTer? |