Canonical Allele Identifier: CA103120417
Gene:

Linked Data

dbSNP Id: rs569599236
gnomAD v2: 4-103422092-CGCA-C
gnomAD v3: 4-102500935-CGCA-C
gnomAD v4: 4-102500935-CGCA-C
MyVariant Identifiers: chr4:g.103422093_103422095del (hg19) chr4:g.102500936_102500938del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500936_102500938del , CM000666.2:g.102500936_102500938del GRCh38
NC_000004.11:g.103422093_103422095del , CM000666.1:g.103422093_103422095del GRCh37
NC_000004.10:g.103641125_103641127del NCBI36
NG_050628.1:g.4608_4610del

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+311_643+313del XP_011530769.1:n.643+311_643+313del
NR_136202.1:n.48+1501_48+1503del
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