HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20888067_20888068insC , CM000684.2:g.20888067_20888068insC | GRCh38 |
NC_000022.10:g.21242355_21242356insC , CM000684.1:g.21242355_21242356insC | GRCh37 |
NC_000022.9:g.19572355_19572356insC | NCBI36 |
NG_012152.1:g.34064_34065insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000215730.12:c.*231_*232insC MANE Select | ENSP00000215730.6:n.*231_*232insC | |
ENST00000215730.11:c.*231_*232insC | ENSP00000215730.6:n.*231_*232insC | |
NM_004782.3:c.*231_*232insC | NP_004773.1:n.*231_*232insC | |
NM_004782.4:c.*231_*232insC MANE Select | NP_004773.1:n.*231_*232insC |