Linked Data
gnomAD v4:
16-2278534-G-GGGCC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2278534_2278535insGGCC , CM000678.2:g.2278534_2278535insGGCC | GRCh38 |
| NC_000016.9:g.2328535_2328536insGGCC , CM000678.1:g.2328535_2328536insGGCC | GRCh37 |
| NC_000016.8:g.2268536_2268537insGGCC | NCBI36 |
| NG_011790.1:g.67212_67213insGGCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301732.10:c.4548-77_4548-76insGGCC MANE Select | ENSP00000301732.5:n.4548-77_4548-76insGGCC | |
| ENST00000301732.9:c.4548-77_4548-76insGGCC | ENSP00000301732.5:n.4548-77_4548-76insGGCC | |
| ENST00000382381.7:c.4374-77_4374-76insGGCC | ENSP00000371818.3:n.4374-77_4374-76insGGCC | |
| ENST00000566200.1:n.1069-77_1069-76insGGCC | ||
| NM_001089.2:c.4548-77_4548-76insGGCC | NP_001080.2:n.4548-77_4548-76insGGCC | |
| NM_001089.3:c.4548-77_4548-76insGGCC MANE Select | NP_001080.2:n.4548-77_4548-76insGGCC |