Linked Data
MyVariant Identifiers:
chr8:g.38001891_38001905del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38144374_38144388del , CM000670.2:g.38144374_38144388del | GRCh38 |
| NC_000008.10:g.38001892_38001906del , CM000670.1:g.38001892_38001906del | GRCh37 |
| NC_000008.9:g.38121049_38121063del | NCBI36 |
| NG_011827.1:g.11697_11711del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000276449.9:c.745_759del | ||
| ENST00000276449.8:c.745_759del | ||
| ENST00000520114.1:n.2714_2728del | ||
| ENST00000522050.1:c.587_601del | ||
| NM_000349.2:c.745_759del | ||
| XM_006716392.1:c.651_665del | ||
| NM_000349.3:c.745_759del |