HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215675643_215675644del , CM000663.2:g.215675643_215675644del | GRCh38 |
NC_000001.10:g.215848985_215848986del , CM000663.1:g.215848985_215848986del | GRCh37 |
NC_000001.9:g.213915608_213915609del | NCBI36 |
NG_009497.1:g.752754_752755del | |
NG_009497.2:g.752806_752807del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.12295-27_12295-26del MANE Select | ENSP00000305941.3:n.12295-27_12295-26del | |
ENST00000674083.1:c.12295-27_12295-26del | ENSP00000501296.1:n.12295-27_12295-26del | |
ENST00000307340.7:c.12295-27_12295-26del | ENSP00000305941.3:n.12295-27_12295-26del | |
NM_206933.2:c.12295-27_12295-26del | NP_996816.2:n.12295-27_12295-26del | |
NM_206933.3:c.12295-27_12295-26del | NP_996816.2:n.12295-27_12295-26del | |
NM_206933.4:c.12295-27_12295-26del MANE Select | NP_996816.3:n.12295-27_12295-26del |