Canonical Allele Identifier: CA566327188
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1358772225
gnomAD v2: 6-30976704-T-C
gnomAD v3: 6-31008927-T-C
gnomAD v4: 6-31008927-T-C
MyVariant Identifiers: chr6:g.30976704T>C (hg19) chr6:g.31008927T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008927T>C , CM000668.2:g.31008927T>C GRCh38
NC_000006.11:g.30976704T>C , CM000668.1:g.30976704T>C GRCh37
NC_000006.10:g.31084683T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1743T>C NP_001185744.1:n.-37-1743T>C
NM_001318484.1:c.8-1778T>C NP_001305413.1:n.8-1778T>C
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