HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94401530dup , CM000669.2:g.94401530dup | GRCh38 |
NC_000007.13:g.94030842dup , CM000669.1:g.94030842dup | GRCh37 |
NC_000007.12:g.93868778dup | NCBI36 |
NG_007405.1:g.11970dup , LRG_2:g.11970dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297268.11:c.226-37dup MANE Select | ENSP00000297268.6:n.226-37dup | |
ENST00000297268.10:c.226-37dup | ENSP00000297268.6:n.226-37dup | |
ENST00000620463.1:c.220-37dup | ENSP00000477719.1:n.220-37dup | |
NM_000089.3:c.226-37dup , LRG_2t1:c.226-37dup | NP_000080.2:n.226-37dup | |
NM_000089.4:c.226-37dup MANE Select | NP_000080.2:n.226-37dup |