Canonical Allele Identifier: CA1618964127
Gene: MUC22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008527C= , CM000668.2:g.31008527C= GRCh38
NC_000006.11:g.30976304C= , CM000668.1:g.30976304C= GRCh37
NC_000006.10:g.31084283C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2143C= NP_001185744.1:n.-37-2143C=
NM_001318484.1:c.8-2178C= NP_001305413.1:n.8-2178C=