Linked Data
gnomAD v4:
14-23421152-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23421154del , CM000676.2:g.23421154del | GRCh38 |
| NC_000014.8:g.23890363del , CM000676.1:g.23890363del | GRCh37 |
| NC_000014.7:g.22960203del | NCBI36 |
| NG_007884.1:g.19509del , LRG_384:g.19509del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.3246-105del MANE Select | ENSP00000347507.3:n.3246-105del | |
| ENST00000355349.3:c.3246-105del | ENSP00000347507.3:n.3246-105del | |
| NM_000257.3:c.3246-105del | NP_000248.2:n.3246-105del | |
| XR_245686.3:n.3354-105del | ||
| XM_017021340.1:c.3246-105del | XP_016876829.1:n.3246-105del | |
| NM_000257.4:c.3246-105del MANE Select | NP_000248.2:n.3246-105del |