Linked Data
gnomAD v4:
19-6713877-G-GC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713883dup , CM000681.2:g.6713883dup | GRCh38 |
| NC_000019.9:g.6713894dup , CM000681.1:g.6713894dup | GRCh37 |
| NC_000019.8:g.6664894dup | NCBI36 |
| NG_009557.1:g.11774dup , LRG_27:g.11774dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.650+114dup | ENSP00000512083.1:n.650+114dup | |
| ENST00000245907.11:c.773+114dup MANE Select | ENSP00000245907.4:n.773+114dup | |
| ENST00000245907.10:c.773+114dup | ENSP00000245907.4:n.773+114dup | |
| ENST00000595577.1:n.277+114dup | ||
| NM_000064.3:c.773+114dup | NP_000055.2:n.773+114dup | |
| NM_000064.4:c.773+114dup MANE Select | NP_000055.2:n.773+114dup |