Canonical Allele Identifier: CA1475304918

Gene:

Linked Data

• dbSNP Id: rs1722644592

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89655638_89655639dup , CM000666.2:g.89655638_89655639dup	GRCh38
NC_000004.11:g.90576789_90576790dup , CM000666.1:g.90576789_90576790dup	GRCh37
NC_000004.10:g.90795812_90795813dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.434+27721_434+27722dup
XR_938987.1:n.688+27721_688+27722dup
XR_938988.1:n.554+27721_554+27722dup
XR_938990.1:n.299-35647_299-35646dup
XR_938991.1:n.434+27721_434+27722dup
XR_938994.1:n.779+27721_779+27722dup
XR_938995.1:n.613+27721_613+27722dup
XR_938986.2:n.459+27721_459+27722dup
XR_938987.2:n.748+27721_748+27722dup