Canonical Allele Identifier: CA569191055
Gene:

Linked Data

dbSNP Id: rs1392439064
gnomAD v2: 6-98550358-GTCTA-G
gnomAD v3: 6-98102482-GTCTA-G
gnomAD v4: 6-98102482-GTCTA-G
MyVariant Identifiers: chr6:g.98550359_98550362del (hg19) chr6:g.98102483_98102486del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102488_98102491del , CM000668.2:g.98102488_98102491del GRCh38
NC_000006.11:g.98550364_98550367del , CM000668.1:g.98550364_98550367del GRCh37
NC_000006.10:g.98657085_98657088del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3218_456+3221del
XR_942809.1:n.456+3218_456+3221del
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Search 100 bp 3'