HGVS | Genome Assembly |
---|---|
NC_000006.12:g.24306150dup , CM000668.2:g.24306150dup | GRCh38 |
NC_000006.11:g.24306378dup , CM000668.1:g.24306378dup | GRCh37 |
NC_000006.10:g.24414357dup | NCBI36 |
NG_012829.1:g.56903dup | |
NG_012829.2:g.82143dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378454.8:c.349-4106dup MANE Select | ENSP00000367715.3:n.349-4106dup | |
ENST00000378454.7:c.349-4106dup | ENSP00000367715.3:n.349-4106dup | |
NM_001195610.1:c.349-4106dup | NP_001182539.1:n.349-4106dup | |
NM_016356.4:c.349-4106dup | NP_057440.2:n.349-4106dup | |
NM_016356.5:c.349-4106dup MANE Select | NP_057440.2:n.349-4106dup | |
NM_001195610.2:c.349-4106dup | NP_001182539.1:n.349-4106dup |