Canonical Allele Identifier: CA817908558
Gene:

Linked Data

dbSNP Id: rs1225109576
gnomAD v3: 6-11943687-CAT-C
gnomAD v4: 6-11943687-CAT-C
MyVariant Identifiers: chr6:g.11943921_11943922del (hg19) chr6:g.11943688_11943689del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943688_11943689del , CM000668.2:g.11943688_11943689del GRCh38
NC_000006.11:g.11943921_11943922del , CM000668.1:g.11943921_11943922del GRCh37
NC_000006.10:g.12051907_12051908del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7847_348-7846del
Search 100 bp 5'
Search 100 bp 3'