Linked Data
gnomAD v4:
6-31357203-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31357206del , CM000668.2:g.31357206del | GRCh38 |
| NC_000006.11:g.31324983del , CM000668.1:g.31324983del | GRCh37 |
| NC_000006.10:g.31432962del | NCBI36 |
| NG_023187.1:g.5009del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.1428del | ||
| ENST00000481849.6:n.1428del | ||
| ENST00000497377.6:n.1428del | ||
| ENST00000696559.1:c.-46del | ENSP00000512717.1:n.-46del | |
| ENST00000696560.1:c.-46del | ENSP00000512718.1:n.-46del | |
| ENST00000696561.1:c.-46del | ENSP00000512719.1:n.-46del | |
| ENST00000696562.1:c.-46del | ENSP00000512720.1:n.-46del | |
| ENST00000603274.1:n.560del | ||
| NM_005514.6:c.-46del | NP_005505.2:n.-46del | |
| NM_005514.7:c.-46del | NP_005505.2:n.-46del |