Linked Data
gnomAD v4:
8-38145895-CA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38145896del , CM000670.2:g.38145896del | GRCh38 |
| NC_000008.10:g.38003414del , CM000670.1:g.38003414del | GRCh37 |
| NC_000008.9:g.38122571del | NCBI36 |
| NG_011827.1:g.10187del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000276449.9:c.650+67del MANE Select | ENSP00000276449.3:n.650+67del | |
| ENST00000276449.8:c.650+67del | ENSP00000276449.3:n.650+67del | |
| ENST00000520114.1:n.1204del | ||
| ENST00000522050.1:c.586+67del | ||
| NM_000349.2:c.650+67del | NP_000340.2:n.650+67del | |
| XM_006716392.1:c.650+67del | XP_006716455.1:n.650+67del | |
| NM_000349.3:c.650+67del MANE Select | NP_000340.2:n.650+67del |