Canonical Allele Identifier: CA1704669367
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46352895T= , CM000669.2:g.46352895T= GRCh38
NC_000007.13:g.46392493T= , CM000669.1:g.46392493T= GRCh37
NC_000007.12:g.46359018T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927241.1:n.3064T=
XR_927242.1:n.2972T=
XR_927241.2:n.3064T=
XR_927242.2:n.3029T=