HGVS | Genome Assembly |
---|---|
NC_000008.11:g.63072900_63072901insT , CM000670.2:g.63072900_63072901insT | GRCh38 |
NC_000008.10:g.63985459_63985460insT , CM000670.1:g.63985459_63985460insT | GRCh37 |
NC_000008.9:g.64148013_64148014insT | NCBI36 |
NG_016123.1:g.18153_18154insA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260116.5:c.358+34_358+35insA MANE Select | ENSP00000260116.4:n.358+34_358+35insA | |
ENST00000260116.4:c.358+34_358+35insA | ENSP00000260116.4:n.358+34_358+35insA | |
ENST00000521138.1:n.232+12917_232+12918insA | ||
NM_000370.3:c.358+34_358+35insA MANE Select | NP_000361.1:n.358+34_358+35insA | |
XM_006716468.2:c.205-8585_205-8584insA | XP_006716531.1:n.205-8585_205-8584insA | |
XM_006716468.4:c.205-8585_205-8584insA | XP_006716531.1:n.205-8585_205-8584insA |