Linked Data
dbSNP Id:
rs1236062782
gnomAD v3:
9-133274203-TCCTCCAGGGCTGCACCTC-T
gnomAD v4:
9-133274203-TCCTCCAGGGCTGCACCTC-T
MyVariant Identifiers:
chr9:g.133274204_133274221del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133274205_133274222del , CM000671.2:g.133274205_133274222del | GRCh38 |
| NC_000009.11:g.136149621_136149638del , CM000671.1:g.136149621_136149638del | GRCh37 |
| NC_000009.10:g.135139442_135139459del | NCBI36 |
| NG_006669.1:g.3414_3431del | |
| NG_006669.2:g.5994_6011del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.58+941_58+958del | ||
| ENST00000647353.1:n.53+941_53+958del | ||
| ENST00000651471.1:n.63+1741_63+1758del | ||
| ENST00000679909.1:c.28+941_28+958del | ENSP00000506089.1:n.28+941_28+958del | |
| ENST00000453660.3:n.40+941_40+958del | ||
| ENST00000538324.2:c.28+941_28+958del | ENSP00000483018.1:n.28+941_28+958del | |
| ENST00000611156.4:c.28+941_28+958del | ENSP00000483265.1:n.28+941_28+958del | |
| NM_020469.2:c.28+941_28+958del | NP_065202.2:n.28+941_28+958del | |
| NM_020469.3:c.28+941_28+958del | NP_065202.2:n.28+941_28+958del |