Canonical Allele Identifier: CA1087405468
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763646399

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008395del , CM000668.2:g.31008395del GRCh38
NC_000006.11:g.30976172del , CM000668.1:g.30976172del GRCh37
NC_000006.10:g.31084151del NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-38+2262del NP_001185744.1:n.-38+2262del
NM_001318484.1:c.7+2262del NP_001305413.1:n.7+2262del