HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10652660_10652661insA , CM000682.2:g.10652660_10652661insA | GRCh38 |
NC_000020.10:g.10633308_10633309insA , CM000682.1:g.10633308_10633309insA | GRCh37 |
NC_000020.9:g.10581308_10581309insA | NCBI36 |
NG_007496.1:g.26386_26387insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254958.10:c.756-63_756-62insT MANE Select | ENSP00000254958.4:n.756-63_756-62insT | |
ENST00000617965.2:n.62_63insT | ||
ENST00000254958.9:c.756-63_756-62insT | ENSP00000254958.4:n.756-63_756-62insT | |
ENST00000423891.6:n.622-63_622-62insT | ||
ENST00000617965.1:n.62_63insT | ||
NM_000214.2:c.756-63_756-62insT | NP_000205.1:n.756-63_756-62insT | |
NM_000214.3:c.756-63_756-62insT MANE Select | NP_000205.1:n.756-63_756-62insT |