HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159316068_159316069insG , CM000667.2:g.159316068_159316069insG | GRCh38 |
NC_000005.9:g.158743076_158743077insG , CM000667.1:g.158743076_158743077insG | GRCh37 |
NC_000005.8:g.158675654_158675655insG | NCBI36 |
NG_009618.1:g.19405_19406insC , LRG_71:g.19405_19406insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.*32_*33insC | ENSP00000512849.1:n.*32_*33insC | |
ENST00000696751.1:c.*514_*515insC | ENSP00000512850.1:n.*514_*515insC | |
ENST00000231228.3:c.*32_*33insC MANE Select | ENSP00000231228.2:n.*32_*33insC | |
ENST00000231228.2:c.*32_*33insC | ENSP00000231228.2:n.*32_*33insC | |
NM_002187.2:c.*32_*33insC , LRG_71t1:c.*32_*33insC | NP_002178.2:n.*32_*33insC | |
NM_002187.3:c.*32_*33insC MANE Select | NP_002178.2:n.*32_*33insC |