HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19117402_19117403insT , CM000669.2:g.19117402_19117403insT | GRCh38 |
NC_000007.13:g.19157025_19157026insT , CM000669.1:g.19157025_19157026insT | GRCh37 |
NC_000007.12:g.19123550_19123551insT | NCBI36 |
NG_008114.1:g.5270_5271insA | |
NG_008114.2:g.5270_5271insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.-82_-81insA MANE Select | ENSP00000242261.5:n.-82_-81insA | |
ENST00000242261.5:c.-82_-81insA | ENSP00000242261.5:n.-82_-81insA | |
NM_000474.3:c.-82_-81insA | NP_000465.1:n.-82_-81insA | |
XM_011515496.1:c.-82_-81insA | XP_011513798.1:n.-82_-81insA | |
NR_149001.1:n.270_271insA | ||
NM_000474.4:c.-82_-81insA MANE Select | NP_000465.1:n.-82_-81insA | |
NR_149001.2:n.234_235insA |