HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32202826_32202827insC , CM000668.2:g.32202826_32202827insC | GRCh38 |
NC_000006.11:g.32170603_32170604insC , CM000668.1:g.32170603_32170604insC | GRCh37 |
NC_000006.10:g.32278581_32278582insC | NCBI36 |
NG_028190.1:g.26241_26242insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.3232-228_3232-227insG MANE Select | ENSP00000364163.3:n.3232-228_3232-227insG | |
ENST00000474612.1:n.1090_1091insG | ||
NM_004557.3:c.3232-228_3232-227insG | NP_004548.3:n.3232-228_3232-227insG | |
NR_134949.1:n.3472+943_3472+944insG | ||
NR_134950.1:n.3370+943_3370+944insG | ||
NM_004557.4:c.3232-228_3232-227insG MANE Select | NP_004548.3:n.3232-228_3232-227insG | |
NR_134949.2:n.3472+943_3472+944insG | ||
NR_134950.2:n.3370+943_3370+944insG |