HGVS | Genome Assembly |
---|---|
NC_000006.12:g.83516729dup , CM000668.2:g.83516729dup | GRCh38 |
NC_000006.11:g.84226448dup , CM000668.1:g.84226448dup | GRCh37 |
NC_000006.10:g.84283167dup | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369700.4:c.-21+4035dup MANE Select | ENSP00000358714.3:n.-21+4035dup | |
ENST00000369700.3:c.-21+4035dup | ENSP00000358714.3:n.-21+4035dup | |
NM_001170423.1:c.-126+4035dup | NP_001163894.1:n.-126+4035dup | |
NM_153362.2:c.-21+4035dup | NP_699193.2:n.-21+4035dup | |
NM_153362.3:c.-21+4035dup MANE Select | NP_699193.2:n.-21+4035dup | |
NM_001170423.2:c.-126+4035dup | NP_001163894.1:n.-126+4035dup |