Canonical Allele Identifier: CA1649534208
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102364A= , CM000668.2:g.98102364A= GRCh38
NC_000006.11:g.98550240A= , CM000668.1:g.98550240A= GRCh37
NC_000006.10:g.98656961A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245563.2:n.456+3094A=
XR_942809.1:n.456+3094A=