Linked Data
gnomAD v3:
6-31463755-G-C
gnomAD v4:
6-31463755-G-C
MyVariant Identifiers:
chr6:g.31431532G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31463755G>C , CM000668.2:g.31463755G>C | GRCh38 |
| NC_000006.11:g.31431532G>C , CM000668.1:g.31431532G>C | GRCh37 |
| NC_000006.10:g.31539511G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_040662.1:n.485G>C |