Linked Data
gnomAD v4:
19-6714312-TA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6714313del , CM000681.2:g.6714313del | GRCh38 |
| NC_000019.9:g.6714324del , CM000681.1:g.6714324del | GRCh37 |
| NC_000019.8:g.6665324del | NCBI36 |
| NG_009557.1:g.11339del , LRG_27:g.11339del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.476+39del | ENSP00000512083.1:n.476+39del | |
| ENST00000245907.11:c.599+39del MANE Select | ENSP00000245907.4:n.599+39del | |
| ENST00000245907.10:c.599+39del | ENSP00000245907.4:n.599+39del | |
| ENST00000595577.1:n.39del | ||
| NM_000064.3:c.599+39del | NP_000055.2:n.599+39del | |
| NM_000064.4:c.599+39del MANE Select | NP_000055.2:n.599+39del |