Canonical Allele Identifier: CA1618964089
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763648950

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008415C>T , CM000668.2:g.31008415C>T GRCh38
NC_000006.11:g.30976192C>T , CM000668.1:g.30976192C>T GRCh37
NC_000006.10:g.31084171C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2255C>T NP_001185744.1:n.-37-2255C>T
NM_001318484.1:c.7+2282C>T NP_001305413.1:n.7+2282C>T