Canonical Allele Identifier: CA799758231

Gene:

Linked Data

• dbSNP Id: rs1178760153
• gnomAD v3: 4-89597911-TG-T
• gnomAD v4: 4-89597911-TG-T
• MyVariant Identifiers: chr4:g.90519063del (hg19) ; chr4:g.89597912del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89597913del , CM000666.2:g.89597913del	GRCh38
NC_000004.11:g.90519064del , CM000666.1:g.90519064del	GRCh37
NC_000004.10:g.90738087del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.298+9973del
XR_938987.1:n.433-240del
XR_938988.1:n.299-240del
XR_938990.1:n.298+9973del
XR_938991.1:n.298+9973del
XR_938992.1:n.298+9973del
XR_938994.1:n.643+9973del
XR_938995.1:n.477+9973del
XR_938996.1:n.298+9973del
XR_938997.1:n.298+9973del
XR_938986.2:n.323+9973del
XR_938987.2:n.493-240del