Canonical Allele Identifier: CA98367567
Gene:

Linked Data

dbSNP Id: rs1040993331
gnomAD v3: 4-62558211-CCTCTT-C
gnomAD v4: 4-62558211-CCTCTT-C
MyVariant Identifiers: chr4:g.63423930_63423934del (hg19) chr4:g.62558212_62558216del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558215_62558219del , CM000666.2:g.62558215_62558219del GRCh38
NC_000004.11:g.63423933_63423937del , CM000666.1:g.63423933_63423937del GRCh37
NC_000004.10:g.63106528_63106532del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5629_161-5625del
Search 100 bp 5'
Search 100 bp 3'