Canonical Allele Identifier: CA1618964295
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763690200

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008877dup , CM000668.2:g.31008877dup GRCh38
NC_000006.11:g.30976654dup , CM000668.1:g.30976654dup GRCh37
NC_000006.10:g.31084633dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1793dup NP_001185744.1:n.-37-1793dup
NM_001318484.1:c.8-1828dup NP_001305413.1:n.8-1828dup