Linked Data
gnomAD v4:
6-31200079-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31200079C>G , CM000668.2:g.31200079C>G | GRCh38 |
| NC_000006.11:g.31167856C>G , CM000668.1:g.31167856C>G | GRCh37 |
| NC_000006.10:g.31275835C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000383331.4:c.123+2197C>G | ||
| ENST00000414008.2:n.186C>G | ||
| ENST00000424675.1:c.44+1898C>G | ||
| NR_026791.1:n.123+2197C>G |