Linked Data
dbSNP Id:
rs1563404074
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.58968486del , CM000670.2:g.58968486del | GRCh38 |
| NC_000008.10:g.59881045del , CM000670.1:g.59881045del | GRCh37 |
| NC_000008.9:g.60043599del | NCBI36 |
| NG_011993.1:g.155728del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361421.2:c.103-8473del MANE Select | ENSP00000354842.1:n.103-8473del | |
| ENST00000361421.1:c.103-8473del | ENSP00000354842.1:n.103-8473del | |
| NM_014729.2:c.103-8473del | NP_055544.1:n.103-8473del | |
| XM_017014085.1:c.103-28937del | XP_016869574.1:n.103-28937del | |
| NM_014729.3:c.103-8473del MANE Select | NP_055544.1:n.103-8473del |