Canonical Allele Identifier:
CA2695783251
Gene:
Linked Data
dbSNP Id:
rs2148777795
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.38158552G>A , CM000663.2:g.38158552G>A | GRCh38 |
| NC_000001.10:g.38624224G>A , CM000663.1:g.38624224G>A | GRCh37 |
| NC_000001.9:g.38396811G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_947202.1:n.45-3141G>A | ||
| XR_947203.1:n.61+16838G>A | ||
| XR_947204.1:n.45-3141G>A | ||
| XR_947205.1:n.45-3141G>A | ||
| XR_001737984.1:n.45-3141G>A | ||
| XR_001737985.1:n.61+16838G>A | ||
| XR_001737986.1:n.45-3141G>A | ||
| XR_001737987.1:n.45-3141G>A | ||
| XR_002958294.1:n.45-3141G>A | ||
| XR_947205.2:n.45-3141G>A |