Canonical Allele Identifier: CA136813370
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs200131340

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008719del , CM000668.2:g.31008719del GRCh38
NC_000006.11:g.30976496del , CM000668.1:g.30976496del GRCh37
NC_000006.10:g.31084475del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1951del NP_001185744.1:n.-37-1951del
NM_001318484.1:c.8-1986del NP_001305413.1:n.8-1986del