Canonical Allele Identifier:
CA1500739590
Gene:
Linked Data
dbSNP Id:
rs1393263322
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144601649A>G , CM000666.2:g.144601649A>G | GRCh38 |
| NC_000004.11:g.145522801A>G , CM000666.1:g.145522801A>G | GRCh37 |
| NC_000004.10:g.145742251A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000649263.1:c.328-185671T>C | ENSP00000497507.1:n.328-185671T>C |