Canonical Allele Identifier: CA566327190
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1399480602
gnomAD v2: 6-30976715-G-GA
gnomAD v3: 6-31008938-G-GA
gnomAD v4: 6-31008938-G-GA
MyVariant Identifiers: chr6:g.30976715_30976716insA (hg19) chr6:g.31008938_31008939insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008939dup , CM000668.2:g.31008939dup GRCh38
NC_000006.11:g.30976716dup , CM000668.1:g.30976716dup GRCh37
NC_000006.10:g.31084695dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1731dup NP_001185744.1:n.-37-1731dup
NM_001318484.1:c.8-1766dup NP_001305413.1:n.8-1766dup
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