Canonical Allele Identifier: CA1087405439
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763641998

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008344del , CM000668.2:g.31008344del GRCh38
NC_000006.11:g.30976121del , CM000668.1:g.30976121del GRCh37
NC_000006.10:g.31084100del NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-38+2211del NP_001185744.1:n.-38+2211del
NM_001318484.1:c.7+2211del NP_001305413.1:n.7+2211del