HGVS | Genome Assembly |
---|---|
NC_000002.12:g.68371797_68371798insC , CM000664.2:g.68371797_68371798insC | GRCh38 |
NC_000002.11:g.68598929_68598930insC , CM000664.1:g.68598929_68598930insC | GRCh37 |
NC_000002.10:g.68452433_68452434insC | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000234313.8:c.42+6404_42+6405insC MANE Select | ENSP00000234313.7:n.42+6404_42+6405insC | |
ENST00000234313.7:c.42+6404_42+6405insC | ENSP00000234313.7:n.42+6404_42+6405insC | |
NM_002664.2:c.42+6404_42+6405insC | NP_002655.2:n.42+6404_42+6405insC | |
XM_011532916.1:c.42+6404_42+6405insC | XP_011531218.1:n.42+6404_42+6405insC | |
NM_002664.3:c.42+6404_42+6405insC MANE Select | NP_002655.2:n.42+6404_42+6405insC |