Linked Data
gnomAD v4:
6-32443704-T-TGTTA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32443705_32443708dup , CM000668.2:g.32443705_32443708dup | GRCh38 |
| NC_000006.11:g.32411482_32411485dup , CM000668.1:g.32411482_32411485dup | GRCh37 |
| NC_000006.10:g.32519460_32519463dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395388.7:c.611-51_611-48dup MANE Select | ENSP00000378786.2:n.611-51_611-48dup | |
| ENST00000374982.5:c.536-51_536-48dup | ENSP00000364121.5:n.536-51_536-48dup | |
| ENST00000395388.6:c.611-51_611-48dup | ENSP00000378786.2:n.611-51_611-48dup | |
| NM_019111.4:c.611-51_611-48dup | NP_061984.2:n.611-51_611-48dup | |
| NM_019111.5:c.611-51_611-48dup MANE Select | NP_061984.2:n.611-51_611-48dup |