Canonical Allele Identifier: CA136813320
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs765296706

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008512_31008513dup , CM000668.2:g.31008512_31008513dup GRCh38
NC_000006.11:g.30976289_30976290dup , CM000668.1:g.30976289_30976290dup GRCh37
NC_000006.10:g.31084268_31084269dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2158_-37-2157dup NP_001185744.1:n.-37-2158_-37-2157dup
NM_001318484.1:c.8-2193_8-2192dup NP_001305413.1:n.8-2193_8-2192dup