Canonical Allele Identifier: CA1704669368
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46352906A= , CM000669.2:g.46352906A= GRCh38
NC_000007.13:g.46392504A= , CM000669.1:g.46392504A= GRCh37
NC_000007.12:g.46359029A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927241.1:n.3075A=
XR_927242.1:n.2983A=
XR_927241.2:n.3075A=
XR_927242.2:n.3040A=