Canonical Allele Identifier: CA1618964086
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763648469

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008412C>A , CM000668.2:g.31008412C>A GRCh38
NC_000006.11:g.30976189C>A , CM000668.1:g.30976189C>A GRCh37
NC_000006.10:g.31084168C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2258C>A NP_001185744.1:n.-37-2258C>A
NM_001318484.1:c.7+2279C>A NP_001305413.1:n.7+2279C>A