Canonical Allele Identifier: CA1618964121
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763655295

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008504C>A , CM000668.2:g.31008504C>A GRCh38
NC_000006.11:g.30976281C>A , CM000668.1:g.30976281C>A GRCh37
NC_000006.10:g.31084260C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-37-2166C>A NP_001185744.1:n.-37-2166C>A
NM_001318484.1:c.8-2201C>A NP_001305413.1:n.8-2201C>A