Linked Data
dbSNP Id:
rs1950102031
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.19626809G>A , CM000674.2:g.19626809G>A | GRCh38 |
| NC_000012.11:g.19779743G>A , CM000674.1:g.19779743G>A | GRCh37 |
| NC_000012.10:g.19671010G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000512223.6:c.339-93824G>A | ENSP00000445587.1:n.339-93824G>A | |
| XR_242921.2:n.252+23496G>A | ||
| XR_931408.1:n.76+803G>A | ||
| XR_001749034.2:n.472-23587G>A | ||
| XR_001749035.1:n.525+23496G>A | ||
| XR_001749036.1:n.526-22889G>A | ||
| XR_001749037.1:n.275+23496G>A | ||
| XR_002957408.1:n.133+803G>A |