Canonical Allele Identifier: CA1475319513
Community Standard Title: NC_000004.12:g.89685446C=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89685446C= , CM000666.2:g.89685446C= GRCh38
NC_000004.11:g.90606597C= , CM000666.1:g.90606597C= GRCh37
NC_000004.10:g.90825620C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741764.1:n.1812C=
XR_001741765.1:n.1230C=
XR_001741766.1:n.233-231C=
XR_938982.1:n.1812C=
XR_938982.2:n.1812C=
XR_938983.1:n.1812C=
XR_938984.1:n.1212C=
XR_938984.2:n.1234C=
XR_938985.1:n.244C=
XR_938985.2:n.266C=
XR_938986.1:n.435-5839C=
XR_938986.2:n.460-5839C=
XR_938987.1:n.689-5839C=
XR_938987.2:n.749-5839C=
XR_938988.1:n.555-5839C=
XR_938989.1:n.210+3762C=
XR_938989.2:n.232+3762C=
XR_938990.1:n.299-5839C=
XR_938991.1:n.435-34380C=
XR_938993.1:n.211-1452C=
XR_938994.1:n.780-5839C=
XR_938995.1:n.614-5839C=