Canonical Allele Identifier: CA799753674

Gene:

Linked Data

• dbSNP Id: rs1192331320
• gnomAD v3: 4-89656020-CAT-C
• gnomAD v4: 4-89656020-CAT-C
• MyVariant Identifiers: chr4:g.90577172_90577173del (hg19) ; chr4:g.89656021_89656022del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89656022_89656023del , CM000666.2:g.89656022_89656023del	GRCh38
NC_000004.11:g.90577173_90577174del , CM000666.1:g.90577173_90577174del	GRCh37
NC_000004.10:g.90796196_90796197del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_938986.1:n.434+28105_434+28106del
XR_938987.1:n.688+28105_688+28106del
XR_938988.1:n.554+28105_554+28106del
XR_938990.1:n.299-35263_299-35262del
XR_938991.1:n.434+28105_434+28106del
XR_938994.1:n.779+28105_779+28106del
XR_938995.1:n.613+28105_613+28106del
XR_938986.2:n.459+28105_459+28106del
XR_938987.2:n.748+28105_748+28106del