Canonical Allele Identifier: CA1618964160
Gene: MUC22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008591C= , CM000668.2:g.31008591C= GRCh38
NC_000006.11:g.30976368C= , CM000668.1:g.30976368C= GRCh37
NC_000006.10:g.31084347C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2079C= NP_001185744.1:n.-37-2079C=
NM_001318484.1:c.8-2114C= NP_001305413.1:n.8-2114C=