Canonical Allele Identifier: CA136813413
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs117712789
gnomAD v2: 6-30976696-G-A
gnomAD v3: 6-31008919-G-A
gnomAD v4: 6-31008919-G-A
MyVariant Identifiers: chr6:g.30976696G>A (hg19) chr6:g.31008919G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008919G>A , CM000668.2:g.31008919G>A GRCh38
NC_000006.11:g.30976696G>A , CM000668.1:g.30976696G>A GRCh37
NC_000006.10:g.31084675G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1751G>A NP_001185744.1:n.-37-1751G>A
NM_001318484.1:c.8-1786G>A NP_001305413.1:n.8-1786G>A
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