Canonical Allele Identifier: CA1704669397
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46352979C= , CM000669.2:g.46352979C= GRCh38
NC_000007.13:g.46392577C= , CM000669.1:g.46392577C= GRCh37
NC_000007.12:g.46359102C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927241.1:n.3148C=
XR_927242.1:n.3056C=
XR_927241.2:n.3148C=
XR_927242.2:n.3113C=