Canonical Allele Identifier: CA823869714
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1431910729
gnomAD v3: 6-31008405-A-AT
gnomAD v4: 6-31008405-A-AT
MyVariant Identifiers: chr6:g.30976182_30976183insT (hg19) chr6:g.31008405_31008406insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008406dup , CM000668.2:g.31008406dup GRCh38
NC_000006.11:g.30976183dup , CM000668.1:g.30976183dup GRCh37
NC_000006.10:g.31084162dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2264dup NP_001185744.1:n.-37-2264dup
NM_001318484.1:c.7+2273dup NP_001305413.1:n.7+2273dup
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