Canonical Allele Identifier: CA144319794
Gene:

Linked Data

dbSNP Id: rs955843689
gnomAD v2: 6-98550379-CT-C
gnomAD v3: 6-98102503-CT-C
gnomAD v4: 6-98102503-CT-C
MyVariant Identifiers: chr6:g.98550380del (hg19) chr6:g.98102504del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102512del , CM000668.2:g.98102512del GRCh38
NC_000006.11:g.98550388del , CM000668.1:g.98550388del GRCh37
NC_000006.10:g.98657109del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3242del
XR_942809.1:n.456+3242del
Search 100 bp 5'
Search 100 bp 3'