Canonical Allele Identifier: CA2538694192

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89655761C>T , CM000666.2:g.89655761C>T	GRCh38
NC_000004.11:g.90576912C>T , CM000666.1:g.90576912C>T	GRCh37
NC_000004.10:g.90795935C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.434+27844C>T
XR_938987.1:n.688+27844C>T
XR_938988.1:n.554+27844C>T
XR_938990.1:n.299-35524C>T
XR_938991.1:n.434+27844C>T
XR_938994.1:n.779+27844C>T
XR_938995.1:n.613+27844C>T
XR_938986.2:n.459+27844C>T
XR_938987.2:n.748+27844C>T