Linked Data
dbSNP Id:
rs1267507411
gnomAD v3:
7-73683467-A-C
gnomAD v4:
7-73683467-A-C
MyVariant Identifiers:
chr7:g.73683467A>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.73683467A>C , CM000669.2:g.73683467A>C | GRCh38 |
| NC_000007.13:g.73097797A>C , CM000669.1:g.73097797A>C | GRCh37 |
| NC_000007.12:g.72735733A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000464615.1:n.359+84A>C |