Canonical Allele Identifier: CA1618964059
Gene: MUC22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008358C= , CM000668.2:g.31008358C= GRCh38
NC_000006.11:g.30976135C= , CM000668.1:g.30976135C= GRCh37
NC_000006.10:g.31084114C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-38+2225C= NP_001185744.1:n.-38+2225C=
NM_001318484.1:c.7+2225C= NP_001305413.1:n.7+2225C=