Canonical Allele Identifier: CA1618964221
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763674588

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008698_31008699del , CM000668.2:g.31008698_31008699del GRCh38
NC_000006.11:g.30976475_30976476del , CM000668.1:g.30976475_30976476del GRCh37
NC_000006.10:g.31084454_31084455del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1972_-37-1971del NP_001185744.1:n.-37-1972_-37-1971del
NM_001318484.1:c.8-2007_8-2006del NP_001305413.1:n.8-2007_8-2006del