Canonical Allele Identifier: CA1142981103
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213682352C= , CM000663.2:g.213682352C= GRCh38
NC_000001.10:g.213855695C= , CM000663.1:g.213855695C= GRCh37
NC_000001.9:g.211922318C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001738463.1:n.601-49065C=
XR_001738464.1:n.426-49065C=