Canonical Allele Identifier: CA101482556

Gene:

Linked Data

• dbSNP Id: rs981120297
• MyVariant Identifiers: chr4:g.90518951A>G (hg19) ; chr4:g.89597800A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89597800A>G , CM000666.2:g.89597800A>G	GRCh38
NC_000004.11:g.90518951A>G , CM000666.1:g.90518951A>G	GRCh37
NC_000004.10:g.90737974A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.298+9860A>G
XR_938987.1:n.433-353A>G
XR_938988.1:n.299-353A>G
XR_938990.1:n.298+9860A>G
XR_938991.1:n.298+9860A>G
XR_938992.1:n.298+9860A>G
XR_938994.1:n.643+9860A>G
XR_938995.1:n.477+9860A>G
XR_938996.1:n.298+9860A>G
XR_938997.1:n.298+9860A>G
XR_938986.2:n.323+9860A>G
XR_938987.2:n.493-353A>G