Linked Data
dbSNP Id:
rs1199983859
gnomAD v3:
6-112069702-T-G
gnomAD v4:
6-112069702-T-G
MyVariant Identifiers:
chr6:g.112069702T>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.112069702T>G , CM000668.2:g.112069702T>G | GRCh38 |
| NC_000006.11:g.112390905T>G , CM000668.1:g.112390905T>G | GRCh37 |
| NC_000006.10:g.112497598T>G | NCBI36 |
| NG_011748.1:g.20628T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361714.5:c.*82T>G | ENSP00000354734.2:n.*82T>G | |
| ENST00000368666.6:c.*82T>G | ENSP00000357655.3:n.*82T>G |