Linked Data
dbSNP Id:
rs972901728
gnomAD v3:
11-134757050-G-A
gnomAD v4:
11-134757050-G-A
MyVariant Identifiers:
chr11:g.134757050G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.134757050G>A , CM000673.2:g.134757050G>A | GRCh38 |
| NC_000011.9:g.134626944G>A , CM000673.1:g.134626944G>A | GRCh37 |
| NC_000011.8:g.134132154G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_147836.1:n.599-4024G>A |