Linked Data
gnomAD v4:
13-48303766-GA-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48303767del , CM000675.2:g.48303767del | GRCh38 |
| NC_000013.10:g.48877903del , CM000675.1:g.48877903del | GRCh37 |
| NC_000013.9:g.47775904del | NCBI36 |
| NG_009009.1:g.5021del , LRG_517:g.5021del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.-146del MANE Select | ENSP00000267163.4:n.-146del | |
| ENST00000646097.1:c.-146del | ENSP00000496556.1:n.-146del | |
| ENST00000650461.1:c.-146del | ENSP00000497193.1:n.-146del | |
| ENST00000525036.1:n.17del | ||
| NM_000321.2:c.-146del , LRG_517t1:c.-146del | NP_000312.2:n.-146del | |
| NM_000321.3:c.-146del MANE Select | NP_000312.2:n.-146del |