HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23423469_23423470insGAG , CM000676.2:g.23423469_23423470insGAG | GRCh38 |
NC_000014.8:g.23892678_23892679insGAG , CM000676.1:g.23892678_23892679insGAG | GRCh37 |
NC_000014.7:g.22962518_22962519insGAG | NCBI36 |
NG_007884.1:g.17192_17193insCTC , LRG_384:g.17192_17193insCTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3099+77_3099+78insCTC MANE Select | ENSP00000347507.3:n.3099+77_3099+78insCTC | |
ENST00000355349.3:c.3099+77_3099+78insCTC | ENSP00000347507.3:n.3099+77_3099+78insCTC | |
NM_000257.3:c.3099+77_3099+78insCTC | NP_000248.2:n.3099+77_3099+78insCTC | |
XR_245686.3:n.3205+77_3205+78insCTC | ||
XM_017021340.1:c.3099+77_3099+78insCTC | XP_016876829.1:n.3099+77_3099+78insCTC | |
NM_000257.4:c.3099+77_3099+78insCTC MANE Select | NP_000248.2:n.3099+77_3099+78insCTC |