Linked Data
dbSNP Id:
rs1555823628
gnomAD v3:
20-35438358-T-TCTCACACACACA
gnomAD v4:
20-35438358-T-TCTCACACACACA
MyVariant Identifiers:
chr20:g.35438358_35438359insCTCACACACACA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.35438359_35438360insTCACACACACAC , CM000682.2:g.35438359_35438360insTCACACACACAC | GRCh38 |
| NC_000020.10:g.34026151_34026152insTCACACACACAC , CM000682.1:g.34026151_34026152insTCACACACACAC | GRCh37 |
| NC_000020.9:g.33489565_33489566insTCACACACACAC | NCBI36 |
| NG_008076.2:g.4861_4862insTGTGTGTGTGAG | |
| NG_008076.3:g.21388_21389insTGTGTGTGTGAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374372.1:c.-241-190_-241-189insTGTGTGTGTGAG | ENSP00000363492.1:n.-241-190_-241-189insTGTGTGTGTGAG | |
| XM_011529075.1:c.-241-190_-241-189insTGTGTGTGTGAG | XP_011527377.1:n.-241-190_-241-189insTGTGTGTGTGAG | |
| XM_011529076.1:c.-241-190_-241-189insTGTGTGTGTGAG | XP_011527378.1:n.-241-190_-241-189insTGTGTGTGTGAG | |
| NM_001319138.1:c.-241-190_-241-189insTGTGTGTGTGAG | NP_001306067.1:n.-241-190_-241-189insTGTGTGTGTGAG | |
| NM_001319138.2:c.-241-190_-241-189insTGTGTGTGTGAG | NP_001306067.1:n.-241-190_-241-189insTGTGTGTGTGAG |