HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23424827_23424829del , CM000676.2:g.23424827_23424829del | GRCh38 |
NC_000014.8:g.23894036_23894038del , CM000676.1:g.23894036_23894038del | GRCh37 |
NC_000014.7:g.22963876_22963878del | NCBI36 |
NG_007884.1:g.15837_15839del , LRG_384:g.15837_15839del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000355349.4:c.2623_2625del MANE Select | ENSP00000347507.3:p.Glu875del | |
ENST00000355349.3:c.2623_2625del | ENSP00000347507.3:p.Glu875del | |
NM_000257.3:c.2623_2625del | NP_000248.2:p.Glu875del | |
XR_245686.3:n.2729_2731del | ||
XM_017021340.1:c.2623_2625del | XP_016876829.1:p.Glu875del | |
NM_000257.4:c.2623_2625del MANE Select | NP_000248.2:p.Glu875del |