Canonical Allele Identifier: CA2838419342
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.77301612T>C , CM000668.2:g.77301612T>C GRCh38
NC_000006.11:g.78011329T>C , CM000668.1:g.78011329T>C GRCh37
NC_000006.10:g.78068048T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241864.3:n.141+15024A>G
XR_942698.1:n.289+15024A>G
XR_001744205.1:n.833+15024A>G
XR_001744206.1:n.835+15024A>G
XR_001744207.1:n.833+15024A>G
XR_241864.4:n.842+15024A>G