HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152304992del , CM000663.2:g.152304992del | GRCh38 |
NC_000001.10:g.152277468del , CM000663.1:g.152277468del | GRCh37 |
NC_000001.9:g.150544092del | NCBI36 |
NG_016190.1:g.25212del , LRG_1028:g.25212del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.9894del MANE Select | ENSP00000357789.1:p.Gly3299GlufsTer? | |
ENST00000368799.1:c.9894del | ENSP00000357789.1:p.Gly3299GlufsTer? | |
NM_002016.1:c.9894del , LRG_1028t1:c.9894del | NP_002007.1:p.Gly3299GlufsTer? | |
XM_011509329.1:c.9108+786del | XP_011507631.1:n.9108+786del | |
NM_002016.2:c.9894del MANE Select | NP_002007.1:p.Gly3299GlufsTer? |