Canonical Allele Identifier: CA2832876109
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036420T>C , CM000663.2:g.2036420T>C GRCh38
NC_000001.10:g.1967859T>C , CM000663.1:g.1967859T>C GRCh37
NC_000001.9:g.1957719T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.773+15A>G
XR_001737845.2:n.791A>G
XR_946823.3:n.776+15A>G