Linked Data
dbSNP Id:
rs11089937
gnomAD v2:
22-22506569-A-C
gnomAD v3:
22-22152176-A-C
gnomAD v4:
22-22152176-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.22152176A>C , CM000684.2:g.22152176A>C | GRCh38 |
| NC_000022.10:g.22506569A>C , CM000684.1:g.22506569A>C | GRCh37 |
| NC_000022.9:g.20836569A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000640991.1:c.203-62945A>C | ENSP00000491969.1:n.203-62945A>C |