HGVS | Genome Assembly |
---|---|
NC_000005.10:g.113387948dup , CM000667.2:g.113387948dup | GRCh38 |
NC_000005.9:g.112723645dup , CM000667.1:g.112723645dup | GRCh37 |
NC_000005.8:g.112751544dup | NCBI36 |
NG_012265.1:g.105883dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000408903.7:c.171-2736dup MANE Select | ENSP00000386227.3:n.171-2736dup | |
ENST00000408903.6:c.171-2736dup | ENSP00000386227.3:n.171-2736dup | |
NM_001085377.1:c.171-2736dup | NP_001078846.1:n.171-2736dup | |
XM_017009473.1:c.171-2736dup | XP_016864962.1:n.171-2736dup | |
NM_001085377.2:c.171-2736dup MANE Select | NP_001078846.2:n.171-2736dup |