HGVS | Genome Assembly |
---|---|
NC_000016.10:g.68737464dup , CM000678.2:g.68737464dup | GRCh38 |
NC_000016.9:g.68771367dup , CM000678.1:g.68771367dup | GRCh37 |
NC_000016.8:g.67328868dup | NCBI36 |
NG_008021.1:g.5173dup , LRG_301:g.5173dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261769.10:c.48+1dup | ||
ENST00000261769.9:c.48+1dup | ||
ENST00000422392.6:c.48+1dup | ||
ENST00000566510.5:c.48+1dup | ||
ENST00000566612.5:c.48+1dup | ||
ENST00000611625.4:c.48+1dup | ||
ENST00000612417.4:c.48+1dup | ||
ENST00000621016.4:c.48+1dup | ||
NM_004360.3:c.48+1dup , LRG_301t1:c.48+1dup | ||
NM_001317184.1:c.48+1dup | ||
NM_001317185.1:c.-1568+1dup | ||
NM_001317186.1:c.-1772+1dup | ||
NM_004360.4:c.48+1dup | ||
NM_004360.5:c.48+1dup | ||
NM_001317184.2:c.48+1dup | ||
NM_001317185.2:c.-1568+1dup | ||
NM_001317186.2:c.-1772+1dup |