Linked Data
dbSNP Id:
rs747937531
ExAC:
5:158750012 CT / C
gnomAD v2:
5-158750012-CT-C
gnomAD v4:
5-159323004-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159323005del , CM000667.2:g.159323005del | GRCh38 |
| NC_000005.9:g.158750013del , CM000667.1:g.158750013del | GRCh37 |
| NC_000005.8:g.158682591del | NCBI36 |
| NG_009618.1:g.12469del , LRG_71:g.12469del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000696750.1:c.-148-2485del | ENSP00000512849.1:n.-148-2485del | |
| ENST00000696751.1:c.364+49del | ENSP00000512850.1:n.364+49del | |
| ENST00000231228.3:c.364+49del MANE Select | ENSP00000231228.2:n.364+49del | |
| ENST00000231228.2:c.364+49del | ENSP00000231228.2:n.364+49del | |
| NM_002187.2:c.364+49del , LRG_71t1:c.364+49del | NP_002178.2:n.364+49del | |
| XR_001742945.1:n.147+2409del | ||
| NM_002187.3:c.364+49del MANE Select | NP_002178.2:n.364+49del |