Canonical Allele Identifier: CA1475304947
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655695T= , CM000666.2:g.89655695T= GRCh38
NC_000004.11:g.90576846T= , CM000666.1:g.90576846T= GRCh37
NC_000004.10:g.90795869T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938986.1:n.434+27778T=
XR_938987.1:n.688+27778T=
XR_938988.1:n.554+27778T=
XR_938990.1:n.299-35590T=
XR_938991.1:n.434+27778T=
XR_938994.1:n.779+27778T=
XR_938995.1:n.613+27778T=
XR_938986.2:n.459+27778T=
XR_938987.2:n.748+27778T=