HGVS | Genome Assembly |
---|---|
NC_000002.12:g.19353056_19353059del , CM000664.2:g.19353056_19353059del | GRCh38 |
NC_000002.11:g.19552817_19552820del , CM000664.1:g.19552817_19552820del | GRCh37 |
NC_000002.10:g.19416298_19416301del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000272223.3:c.665+82_665+85del MANE Select | ENSP00000272223.2:n.665+82_665+85del | |
ENST00000272223.2:c.665+82_665+85del | ENSP00000272223.2:n.665+82_665+85del | |
ENST00000487581.1:n.3772+82_3772+85del | ||
NM_145260.2:c.665+82_665+85del | NP_660303.1:n.665+82_665+85del | |
XM_006711942.2:c.665+82_665+85del | XP_006712005.1:n.665+82_665+85del | |
XM_006711942.4:c.665+82_665+85del | XP_006712005.1:n.665+82_665+85del | |
NM_145260.3:c.665+82_665+85del MANE Select | NP_660303.1:n.665+82_665+85del |