Linked Data
dbSNP Id:
rs1562175610
gnomAD v2:
6-31325028-A-ACGCG
gnomAD v4:
6-31357251-A-ACGCG
MyVariant Identifiers:
chr6:g.31325028_31325029insCGCG (hg19)
chr6:g.31357251_31357252insCGCG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31357251_31357252insCGCG , CM000668.2:g.31357251_31357252insCGCG | GRCh38 |
| NC_000006.11:g.31325028_31325029insCGCG , CM000668.1:g.31325028_31325029insCGCG | GRCh37 |
| NC_000006.10:g.31433007_31433008insCGCG | NCBI36 |
| NG_023187.1:g.4961_4962insCGCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.1380_1381insCGCG | ||
| ENST00000481849.6:n.1380_1381insCGCG | ||
| ENST00000497377.6:n.1380_1381insCGCG | ||
| ENST00000696559.1:c.-94_-93insCGCG | ENSP00000512717.1:n.-94_-93insCGCG | |
| ENST00000696560.1:c.-94_-93insCGCG | ENSP00000512718.1:n.-94_-93insCGCG | |
| ENST00000696561.1:c.-94_-93insCGCG | ENSP00000512719.1:n.-94_-93insCGCG | |
| ENST00000696562.1:c.-94_-93insCGCG | ENSP00000512720.1:n.-94_-93insCGCG | |
| ENST00000603274.1:n.605_606insCGCG |