Linked Data
dbSNP Id:
rs1157473854
gnomAD v4:
6-112069690-T-C
MyVariant Identifiers:
chr6:g.112069690T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.112069690T>C , CM000668.2:g.112069690T>C | GRCh38 |
| NC_000006.11:g.112390893T>C , CM000668.1:g.112390893T>C | GRCh37 |
| NC_000006.10:g.112497586T>C | NCBI36 |
| NG_011748.1:g.20616T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361714.5:c.*70T>C | ENSP00000354734.2:n.*70T>C | |
| ENST00000368666.6:c.*70T>C | ENSP00000357655.3:n.*70T>C |