Canonical Allele Identifier: CA1649534217
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102391G= , CM000668.2:g.98102391G= GRCh38
NC_000006.11:g.98550267G= , CM000668.1:g.98550267G= GRCh37
NC_000006.10:g.98656988G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3121G=
XR_942809.1:n.456+3121G=