Linked Data
dbSNP Id:
rs1397484980
gnomAD v2:
9-96929718-G-GTAAA
gnomAD v3:
9-94167436-G-GTAAA
gnomAD v4:
9-94167436-G-GTAAA
MyVariant Identifiers:
chr9:g.96929718_96929719insTAAA (hg19)
chr9:g.94167436_94167437insTAAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.94167438_94167441dup , CM000671.2:g.94167438_94167441dup | GRCh38 |
| NC_000009.11:g.96929720_96929723dup , CM000671.1:g.96929720_96929723dup | GRCh37 |
| NC_000009.10:g.95969541_95969544dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_170274.1:n.124+1057_124+1060dup | ||
| NR_170275.1:n.124+1057_124+1060dup | ||
| NR_170276.1:n.124+1057_124+1060dup | ||
| NR_170277.1:n.124+1057_124+1060dup | ||
| NR_170278.1:n.124+1057_124+1060dup |