Canonical Allele Identifier: CA553236610

Gene:

Linked Data

• dbSNP Id: rs1226374577
• gnomAD v2: 4-90576940-CTG-C
• gnomAD v3: 4-89655789-CTG-C
• gnomAD v4: 4-89655789-CTG-C
• MyVariant Identifiers: chr4:g.90576941_90576942del (hg19) ; chr4:g.89655790_89655791del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89655793_89655794del , CM000666.2:g.89655793_89655794del	GRCh38
NC_000004.11:g.90576944_90576945del , CM000666.1:g.90576944_90576945del	GRCh37
NC_000004.10:g.90795967_90795968del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.434+27876_434+27877del
XR_938987.1:n.688+27876_688+27877del
XR_938988.1:n.554+27876_554+27877del
XR_938990.1:n.299-35492_299-35491del
XR_938991.1:n.434+27876_434+27877del
XR_938994.1:n.779+27876_779+27877del
XR_938995.1:n.613+27876_613+27877del
XR_938986.2:n.459+27876_459+27877del
XR_938987.2:n.748+27876_748+27877del