Canonical Allele Identifier: CA569179919
Gene:

Linked Data

dbSNP Id: rs5878504
gnomAD v2: 6-98462624-ATT-A
gnomAD v3: 6-98014748-ATT-A
gnomAD v4: 6-98014748-ATT-A
MyVariant Identifiers: chr6:g.98462629_98462630del (hg19) chr6:g.98462625_98462626del (hg19) chr6:g.98014753_98014754del (hg38) chr6:g.98014749_98014750del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014761_98014762del , CM000668.2:g.98014761_98014762del GRCh38
NC_000006.11:g.98462637_98462638del , CM000668.1:g.98462637_98462638del GRCh37
NC_000006.10:g.98569358_98569359del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45295_371+45296del
XR_942809.1:n.371+45295_371+45296del
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