Canonical Allele Identifier: CA1732839040
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107862996A= , CM000669.2:g.107862996A= GRCh38
NC_000007.13:g.107503441A= , CM000669.1:g.107503441A= GRCh37
NC_000007.12:g.107290677A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927850.1:n.41-821T=
XR_927850.2:n.41-821T=