Canonical Allele Identifier: CA1704669395
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46352977T= , CM000669.2:g.46352977T= GRCh38
NC_000007.13:g.46392575T= , CM000669.1:g.46392575T= GRCh37
NC_000007.12:g.46359100T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927241.1:n.3146T=
XR_927242.1:n.3054T=
XR_927241.2:n.3146T=
XR_927242.2:n.3111T=