Canonical Allele Identifier: CA1215889112
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192571891G>C , CM000663.2:g.192571891G>C GRCh38
NC_000001.10:g.192541021G>C , CM000663.1:g.192541021G>C GRCh37
NC_000001.9:g.190807644G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922382.1:n.267-4675C>G
XR_002958418.1:n.288-4675C>G