Canonical Allele Identifier: CA1649498078
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014449G= , CM000668.2:g.98014449G= GRCh38
NC_000006.11:g.98462325G= , CM000668.1:g.98462325G= GRCh37
NC_000006.10:g.98569046G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+44983G=
XR_942809.1:n.371+44983G=