Canonical Allele Identifier: CA136813400
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1036162063
gnomAD v2: 6-30976641-A-G
gnomAD v3: 6-31008864-A-G
gnomAD v4: 6-31008864-A-G
MyVariant Identifiers: chr6:g.30976641A>G (hg19) chr6:g.31008864A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008864A>G , CM000668.2:g.31008864A>G GRCh38
NC_000006.11:g.30976641A>G , CM000668.1:g.30976641A>G GRCh37
NC_000006.10:g.31084620A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1806A>G NP_001185744.1:n.-37-1806A>G
NM_001318484.1:c.8-1841A>G NP_001305413.1:n.8-1841A>G
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