Canonical Allele Identifier: CA2838419340
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.77292028T>C , CM000668.2:g.77292028T>C GRCh38
NC_000006.11:g.78001745T>C , CM000668.1:g.78001745T>C GRCh37
NC_000006.10:g.78058464T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_241864.3:n.142-18721A>G
XR_942698.1:n.290-18721A>G
XR_001744205.1:n.834-18721A>G
XR_001744206.1:n.836-18721A>G
XR_001744207.1:n.834-18721A>G
XR_241864.4:n.843-18721A>G