Linked Data
dbSNP Id:
rs1481639330
gnomAD v2:
6-148117096-A-ATAT
gnomAD v3:
6-147795960-A-ATAT
gnomAD v4:
6-147795960-A-ATAT
MyVariant Identifiers:
chr6:g.148117096_148117097insTAT (hg19)
chr6:g.147795960_147795961insTAT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.147795963_147795965dup , CM000668.2:g.147795963_147795965dup | GRCh38 |
| NC_000006.11:g.148117099_148117101dup , CM000668.1:g.148117099_148117101dup | GRCh37 |
| NC_000006.10:g.148158792_148158794dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017010850.1:c.460-151509_460-151507dup | XP_016866339.1:n.460-151509_460-151507dup |