Canonical Allele Identifier: CA136813329
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs901181727

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008537_31008559del , CM000668.2:g.31008537_31008559del GRCh38
NC_000006.11:g.30976314_30976336del , CM000668.1:g.30976314_30976336del GRCh37
NC_000006.10:g.31084293_31084315del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2133_-37-2111del NP_001185744.1:n.-37-2133_-37-2111del
NM_001318484.1:c.8-2168_8-2146del NP_001305413.1:n.8-2168_8-2146del