Canonical Allele Identifier: CA77246681
Gene:

Linked Data

dbSNP Id: rs200478393
gnomAD v2: 3-72316019-ACACT-A
gnomAD v3: 3-72266868-ACACT-A
gnomAD v4: 3-72266868-ACACT-A
MyVariant Identifiers: chr3:g.72316020_72316023del (hg19) chr3:g.72266869_72266872del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.72266869_72266872del , CM000665.2:g.72266869_72266872del GRCh38
NC_000003.11:g.72316020_72316023del , CM000665.1:g.72316020_72316023del GRCh37
NC_000003.10:g.72398710_72398713del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940958.1:n.835+8236_835+8239del
Search 100 bp 5'
Search 100 bp 3'