Canonical Allele Identifier: CA1618964060
Gene: MUC22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008364T= , CM000668.2:g.31008364T= GRCh38
NC_000006.11:g.30976141T= , CM000668.1:g.30976141T= GRCh37
NC_000006.10:g.31084120T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-38+2231T= NP_001185744.1:n.-38+2231T=
NM_001318484.1:c.7+2231T= NP_001305413.1:n.7+2231T=