Linked Data
dbSNP Id:
rs1776647648
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.109305560_109305563del , CM000668.2:g.109305560_109305563del | GRCh38 |
| NC_000006.11:g.109626763_109626766del , CM000668.1:g.109626763_109626766del | GRCh37 |
| NC_000006.10:g.109733456_109733459del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000429614.6:n.323-399_323-396del | ||
| ENST00000689724.1:n.55-399_55-396del | ||
| ENST00000691019.1:n.505-399_505-396del | ||
| ENST00000691264.1:n.61-399_61-396del | ||
| ENST00000693346.1:n.55-399_55-396del | ||
| ENST00000368966.10:n.4200-399_4200-396del | ||
| ENST00000638844.1:n.456-399_456-396del | ||
| ENST00000368966.8:n.456-399_456-396del | ||
| ENST00000422819.5:n.462-399_462-396del | ||
| ENST00000429614.5:n.323-399_323-396del | ||
| ENST00000615766.4:n.825-399_825-396del | ||
| NR_028595.1:n.323-399_323-396del | ||
| NR_152435.1:n.4168-399_4168-396del |