HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86739898_86739899insACA , CM000670.2:g.86739898_86739899insACA | GRCh38 |
NC_000008.10:g.87752126_87752127insACA , CM000670.1:g.87752126_87752127insACA | GRCh37 |
NC_000008.9:g.87821242_87821243insACA | NCBI36 |
NG_016980.1:g.8777_8778insTGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.130-163_130-162insTGT MANE Select | ENSP00000316605.5:n.130-163_130-162insTGT | |
ENST00000681746.1:c.130-163_130-162insTGT | ENSP00000505959.1:n.130-163_130-162insTGT | |
ENST00000320005.5:c.130-163_130-162insTGT | ENSP00000316605.5:n.130-163_130-162insTGT | |
ENST00000519777.1:n.112-163_112-162insTGT | ||
NM_019098.4:c.130-163_130-162insTGT | NP_061971.3:n.130-163_130-162insTGT | |
NM_019098.5:c.130-163_130-162insTGT MANE Select | NP_061971.3:n.130-163_130-162insTGT |