HGVS | Genome Assembly |
---|---|
NC_000009.12:g.77794236_77794237delinsTA , CM000671.2:g.77794236_77794237delinsTA | GRCh38 |
NC_000009.11:g.80409152_80409153delinsTA , CM000671.1:g.80409152_80409153delinsTA | GRCh37 |
NC_000009.10:g.79598972_79598973delinsTA | NCBI36 |
NG_027904.2:g.242067_242068delinsTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286548.9:c.735+226_735+227delinsTA MANE Select | ENSP00000286548.4:n.735+226_735+227delinsTA | |
ENST00000286548.8:c.735+226_735+227delinsTA | ENSP00000286548.4:n.735+226_735+227delinsTA | |
NM_002072.4:c.735+226_735+227delinsTA | NP_002063.2:n.735+226_735+227delinsTA | |
XM_017014628.2:c.561+226_561+227delinsTA | XP_016870117.1:n.561+226_561+227delinsTA | |
NM_002072.5:c.735+226_735+227delinsTA MANE Select | NP_002063.2:n.735+226_735+227delinsTA |