HGVS | Genome Assembly |
---|---|
NC_000003.12:g.181713575dup , CM000665.2:g.181713575dup | GRCh38 |
NC_000003.11:g.181431363dup , CM000665.1:g.181431363dup | GRCh37 |
NC_000003.10:g.182914057dup | NCBI36 |
NG_009080.1:g.6642dup , LRG_719:g.6642dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325404.3:c.*261dup (SOX2) MANE Select | ENSP00000323588.1:n.*261dup | |
ENST00000325404.2:c.*261dup (SOX2) | ENSP00000323588.1:n.*261dup | |
NM_003106.3:c.*261dup (SOX2) | NP_003097.1:n.*261dup | |
NR_004053.3:n.768-1610dup (SOX2-OT) | ||
NR_075089.1:n.767+13692dup (SOX2-OT) | ||
NR_075090.1:n.482-25994dup (SOX2-OT) | ||
NR_075091.1:n.783-1610dup (SOX2-OT) | ||
NR_075092.1:n.782+13692dup (SOX2-OT) | ||
NR_075093.1:n.473-25994dup (SOX2-OT) | ||
NM_003106.4:c.*261dup (SOX2) MANE Select | NP_003097.1:n.*261dup |