Canonical Allele Identifier: CA101489327

Gene:

Linked Data

• dbSNP Id: rs915727217
• MyVariant Identifiers: chr4:g.90576745C>G (hg19) ; chr4:g.89655594C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89655594C>G , CM000666.2:g.89655594C>G	GRCh38
NC_000004.11:g.90576745C>G , CM000666.1:g.90576745C>G	GRCh37
NC_000004.10:g.90795768C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.434+27677C>G
XR_938987.1:n.688+27677C>G
XR_938988.1:n.554+27677C>G
XR_938990.1:n.299-35691C>G
XR_938991.1:n.434+27677C>G
XR_938994.1:n.779+27677C>G
XR_938995.1:n.613+27677C>G
XR_938986.2:n.459+27677C>G
XR_938987.2:n.748+27677C>G