Linked Data
dbSNP Id:
rs529876555
gnomAD v2:
9-88699993-C-CA
gnomAD v3:
9-86085078-C-CA
gnomAD v4:
9-86085078-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.86085086dup , CM000671.2:g.86085086dup | GRCh38 |
| NC_000009.11:g.88700001dup , CM000671.1:g.88700001dup | GRCh37 |
| NC_000009.10:g.87889821dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000388711.7:c.-21-5738dup | ENSP00000373363.3:n.-21-5738dup | |
| ENST00000388712.7:c.-21-5738dup MANE Select | ENSP00000373364.3:n.-21-5738dup | |
| ENST00000466178.1:c.-141-40dup | ENSP00000418155.1:n.-141-40dup | |
| ENST00000472919.1:n.150-5738dup | ||
| NM_016548.3:c.-21-5738dup | NP_057632.2:n.-21-5738dup | |
| NM_177937.2:c.-21-5738dup | NP_808800.1:n.-21-5738dup | |
| NM_016548.4:c.-21-5738dup MANE Select | NP_057632.2:n.-21-5738dup | |
| NM_177937.3:c.-21-5738dup | NP_808800.1:n.-21-5738dup |