Canonical Allele Identifier: CA1087405721
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1581592498
gnomAD v3: 6-31008576-T-G
gnomAD v4: 6-31008576-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008576T>G , CM000668.2:g.31008576T>G GRCh38
NC_000006.11:g.30976353T>G , CM000668.1:g.30976353T>G GRCh37
NC_000006.10:g.31084332T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2094T>G NP_001185744.1:n.-37-2094T>G
NM_001318484.1:c.8-2129T>G NP_001305413.1:n.8-2129T>G
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