Canonical Allele Identifier: CA101489330

Gene:

Linked Data

• dbSNP Id: rs73833507
• gnomAD v2: 4-90576782-C-A
• gnomAD v3: 4-89655631-C-A
• gnomAD v4: 4-89655631-C-A
• MyVariant Identifiers: chr4:g.90576782C>A (hg19) ; chr4:g.89655631C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89655631C>A , CM000666.2:g.89655631C>A	GRCh38
NC_000004.11:g.90576782C>A , CM000666.1:g.90576782C>A	GRCh37
NC_000004.10:g.90795805C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.434+27714C>A
XR_938987.1:n.688+27714C>A
XR_938988.1:n.554+27714C>A
XR_938990.1:n.299-35654C>A
XR_938991.1:n.434+27714C>A
XR_938994.1:n.779+27714C>A
XR_938995.1:n.613+27714C>A
XR_938986.2:n.459+27714C>A
XR_938987.2:n.748+27714C>A