Linked Data
dbSNP Id:
rs1200940710
gnomAD v3:
22-42126338-T-TG
gnomAD v4:
22-42126338-T-TG
MyVariant Identifiers:
chr22:g.42126338_42126339insG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42126343dup , CM000684.2:g.42126343dup | GRCh38 |
| NC_000022.10:g.42522345dup , CM000684.1:g.42522345dup | GRCh37 |
| NC_000022.9:g.40852289dup | NCBI36 |
| NG_008376.3:g.8653dup | |
| NG_008376.4:g.9472dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011529966.1:c.1452+277dup | XP_011528268.1:n.1452+277dup | |
| XM_011529967.1:c.1452+277dup | XP_011528269.1:n.1452+277dup | |
| XM_011529968.1:c.1452+277dup | XP_011528270.1:n.1452+277dup | |
| XM_011529969.1:c.1308+277dup | XP_011528271.1:n.1308+277dup | |
| XM_011529970.1:c.1299+277dup | XP_011528272.1:n.1299+277dup |