Canonical Allele Identifier: CA1649534298
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102565C= , CM000668.2:g.98102565C= GRCh38
NC_000006.11:g.98550441C= , CM000668.1:g.98550441C= GRCh37
NC_000006.10:g.98657162C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3295C=
XR_942809.1:n.456+3295C=