Canonical Allele Identifier: CA1475304922

Gene:

Linked Data

• dbSNP Id: rs1578094417

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89655639G>C , CM000666.2:g.89655639G>C	GRCh38
NC_000004.11:g.90576790G>C , CM000666.1:g.90576790G>C	GRCh37
NC_000004.10:g.90795813G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_938986.1:n.434+27722G>C
XR_938987.1:n.688+27722G>C
XR_938988.1:n.554+27722G>C
XR_938990.1:n.299-35646G>C
XR_938991.1:n.434+27722G>C
XR_938994.1:n.779+27722G>C
XR_938995.1:n.613+27722G>C
XR_938986.2:n.459+27722G>C
XR_938987.2:n.748+27722G>C