HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152304672dup , CM000663.2:g.152304672dup | GRCh38 |
NC_000001.10:g.152277148dup , CM000663.1:g.152277148dup | GRCh37 |
NC_000001.9:g.150543772dup | NCBI36 |
NG_016190.1:g.25533dup , LRG_1028:g.25533dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000368799.2:c.10215dup MANE Select | ENSP00000357789.1:p.Ser3406GlnfsTer? | |
ENST00000368799.1:c.10215dup | ENSP00000357789.1:p.Ser3406GlnfsTer? | |
NM_002016.1:c.10215dup , LRG_1028t1:c.10215dup | NP_002007.1:p.Ser3406GlnfsTer? | |
XM_011509329.1:c.9109-838dup | XP_011507631.1:n.9109-838dup | |
NM_002016.2:c.10215dup MANE Select | NP_002007.1:p.Ser3406GlnfsTer? |