Canonical Allele Identifier: CA1618964032
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763638262

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008256dup , CM000668.2:g.31008256dup GRCh38
NC_000006.11:g.30976033dup , CM000668.1:g.30976033dup GRCh37
NC_000006.10:g.31084012dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-38+2123dup NP_001185744.1:n.-38+2123dup
NM_001318484.1:c.7+2123dup NP_001305413.1:n.7+2123dup