HGVS | Genome Assembly |
---|---|
NC_000008.11:g.10612977dup , CM000670.2:g.10612977dup | GRCh38 |
NC_000008.10:g.10470487dup , CM000670.1:g.10470487dup | GRCh37 |
NC_000008.9:g.10507897dup | NCBI36 |
NG_028035.1:g.47134dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382483.4:c.1124dup MANE Select | ENSP00000371923.3:p.Phe376LeufsTer? | |
ENST00000382483.3:c.1124dup | ENSP00000371923.3:p.Phe376LeufsTer? | |
NM_178857.5:c.1124dup | NP_849188.4:p.Phe376LeufsTer? | |
NM_178857.6:c.1124dup MANE Select | NP_849188.4:p.Phe376LeufsTer? |