Canonical Allele Identifier: CA1649534279
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102514A= , CM000668.2:g.98102514A= GRCh38
NC_000006.11:g.98550390A= , CM000668.1:g.98550390A= GRCh37
NC_000006.10:g.98657111A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3244A=
XR_942809.1:n.456+3244A=