HGVS | Genome Assembly |
---|---|
NC_000023.11:g.43949471_43949472del , CM000685.2:g.43949471_43949472del | GRCh38 |
NC_000023.10:g.43808717_43808718del , CM000685.1:g.43808717_43808718del | GRCh37 |
NC_000023.9:g.43693661_43693662del | NCBI36 |
NG_009832.1:g.29206_29207del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000642620.1:c.*329_*330del MANE Select | ENSP00000495972.1:n.*329_*330del | |
ENST00000647044.1:c.*329_*330del | ENSP00000495811.1:n.*329_*330del | |
ENST00000378062.5:c.*329_*330del | ENSP00000367301.5:n.*329_*330del | |
NM_000266.3:c.*329_*330del | NP_000257.1:n.*329_*330del | |
NM_000266.4:c.*329_*330del MANE Select | NP_000257.1:n.*329_*330del |