HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4862680_4862686dup , CM000666.2:g.4862680_4862686dup | GRCh38 |
NC_000004.11:g.4864407_4864413dup , CM000666.1:g.4864407_4864413dup | GRCh37 |
NC_000004.10:g.4915308_4915314dup | NCBI36 |
NG_008121.1:g.8016_8022dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.470-21_470-15dup MANE Select | ENSP00000372170.4:n.470-21_470-15dup | |
ENST00000382723.4:c.470-21_470-15dup | ENSP00000372170.4:n.470-21_470-15dup | |
ENST00000468421.1:n.182-21_182-15dup | ||
NM_002448.3:c.470-21_470-15dup MANE Select | NP_002439.2:n.470-21_470-15dup |