Linked Data
dbSNP Id:
rs1696098774
gnomAD v2:
3-10183240-T-TAAAAA
gnomAD v3:
3-10141556-T-TAAAAA
gnomAD v4:
3-10141556-T-TAAAAA
MyVariant Identifiers:
chr3:g.10183240_10183241insAAAAA (hg19)
chr3:g.10141556_10141557insAAAAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10141556_10141557insAAAAA , CM000665.2:g.10141556_10141557insAAAAA | GRCh38 |
| NC_000003.11:g.10183240_10183241insAAAAA , CM000665.1:g.10183240_10183241insAAAAA | GRCh37 |
| NC_000003.10:g.10158240_10158241insAAAAA | NCBI36 |
| NG_008212.3:g.4922_4923insAAAAA , LRG_322:g.4922_4923insAAAAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256474.2:c.-292_-291insAAAAA | ENSP00000256474.2:n.-292_-291insAAAAA |