Canonical Allele Identifier: CA101482559

Gene:

Linked Data

• dbSNP Id: rs937235700
• MyVariant Identifiers: chr4:g.90518994A>T (hg19) ; chr4:g.89597843A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89597843A>T , CM000666.2:g.89597843A>T	GRCh38
NC_000004.11:g.90518994A>T , CM000666.1:g.90518994A>T	GRCh37
NC_000004.10:g.90738017A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_938986.1:n.298+9903A>T
XR_938987.1:n.433-310A>T
XR_938988.1:n.299-310A>T
XR_938990.1:n.298+9903A>T
XR_938991.1:n.298+9903A>T
XR_938992.1:n.298+9903A>T
XR_938994.1:n.643+9903A>T
XR_938995.1:n.477+9903A>T
XR_938996.1:n.298+9903A>T
XR_938997.1:n.298+9903A>T
XR_938986.2:n.323+9903A>T
XR_938987.2:n.493-310A>T