Linked Data
dbSNP Id:
rs150854274
gnomAD v2:
6-32432695-G-GTTTT
gnomAD v3:
6-32464918-G-GTTTT
gnomAD v4:
6-32464918-G-GTTTT
MyVariant Identifiers:
chr6:g.32432695_32432696insTTTT (hg19)
chr6:g.32464918_32464919insTTTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32464923_32464926dup , CM000668.2:g.32464923_32464926dup | GRCh38 |
| NC_000006.11:g.32432700_32432703dup , CM000668.1:g.32432700_32432703dup | GRCh37 |
| NC_000006.10:g.32540678_32540681dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000449413.1:n.77-4835_77-4832dup |