Canonical Allele Identifier: CA1618964313
Gene: MUC22 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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