Canonical Allele Identifier: CA136813344
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs958772656
gnomAD v2: 6-30976332-T-TC
gnomAD v3: 6-31008555-T-TC
gnomAD v4: 6-31008555-T-TC
MyVariant Identifiers: chr6:g.30976332_30976333insC (hg19) chr6:g.31008555_31008556insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008555_31008556insC , CM000668.2:g.31008555_31008556insC GRCh38
NC_000006.11:g.30976332_30976333insC , CM000668.1:g.30976332_30976333insC GRCh37
NC_000006.10:g.31084311_31084312insC NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2115_-37-2114insC NP_001185744.1:n.-37-2115_-37-2114insC
NM_001318484.1:c.8-2150_8-2149insC NP_001305413.1:n.8-2150_8-2149insC
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