Canonical Allele Identifier: CA10667802
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34285335T>C , CM000663.2:g.34285335T>C GRCh38
NC_000001.10:g.34750936T>C , CM000663.1:g.34750936T>C GRCh37
NC_000001.9:g.34523523T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947169.1:n.493+4328T>C
XR_947169.2:n.493+4328T>C