Canonical Allele Identifier: CA16258579
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs9262458
gnomAD v2: 6-30976660-C-T
gnomAD v3: 6-31008883-C-T
gnomAD v4: 6-31008883-C-T
MyVariant Identifiers: chr6:g.30976660C>T (hg19) chr6:g.31008883C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008883C>T , CM000668.2:g.31008883C>T GRCh38
NC_000006.11:g.30976660C>T , CM000668.1:g.30976660C>T GRCh37
NC_000006.10:g.31084639C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1787C>T NP_001185744.1:n.-37-1787C>T
NM_001318484.1:c.8-1822C>T NP_001305413.1:n.8-1822C>T
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