HGVS | Genome Assembly |
---|---|
NC_000006.12:g.49459509_49459510delinsGA , CM000668.2:g.49459509_49459510delinsGA | GRCh38 |
NC_000006.11:g.49427222_49427223delinsGA , CM000668.1:g.49427222_49427223delinsGA | GRCh37 |
NC_000006.10:g.49535181_49535182delinsGA | NCBI36 |
NG_007100.1:g.8630_8631delinsTC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274813.4:c.-39-5_-39-4delinsTC MANE Select | ENSP00000274813.3:n.-39-5_-39-4delinsTC | |
ENST00000274813.3:c.-39-5_-39-4delinsTC | ENSP00000274813.3:n.-39-5_-39-4delinsTC | |
NM_000255.3:c.-39-5_-39-4delinsTC | NP_000246.2:n.-39-5_-39-4delinsTC | |
XM_005249143.2:c.-39-5_-39-4delinsTC | XP_005249200.1:n.-39-5_-39-4delinsTC | |
XM_005249143.3:c.-39-5_-39-4delinsTC | XP_005249200.1:n.-39-5_-39-4delinsTC | |
NM_000255.4:c.-39-5_-39-4delinsTC MANE Select | NP_000246.2:n.-39-5_-39-4delinsTC |