Linked Data
gnomAD v4:
14-23423837-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23423840del , CM000676.2:g.23423840del | GRCh38 |
| NC_000014.8:g.23893049del , CM000676.1:g.23893049del | GRCh37 |
| NC_000014.7:g.22962889del | NCBI36 |
| NG_007884.1:g.16824del , LRG_384:g.16824del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.2922+69del MANE Select | ENSP00000347507.3:n.2922+69del | |
| ENST00000355349.3:c.2922+69del | ENSP00000347507.3:n.2922+69del | |
| NM_000257.3:c.2922+69del | NP_000248.2:n.2922+69del | |
| XR_245686.3:n.3028+69del | ||
| XM_017021340.1:c.2922+69del | XP_016876829.1:n.2922+69del | |
| NM_000257.4:c.2922+69del MANE Select | NP_000248.2:n.2922+69del |