Canonical Allele Identifier: CA1475305025
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655849C= , CM000666.2:g.89655849C= GRCh38
NC_000004.11:g.90577000C= , CM000666.1:g.90577000C= GRCh37
NC_000004.10:g.90796023C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+27932C=
XR_938987.1:n.688+27932C=
XR_938988.1:n.554+27932C=
XR_938990.1:n.299-35436C=
XR_938991.1:n.434+27932C=
XR_938994.1:n.779+27932C=
XR_938995.1:n.613+27932C=
XR_938986.2:n.459+27932C=
XR_938987.2:n.748+27932C=