Canonical Allele Identifier: CA136813310
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs772352077

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008482_31008483del , CM000668.2:g.31008482_31008483del GRCh38
NC_000006.11:g.30976259_30976260del , CM000668.1:g.30976259_30976260del GRCh37
NC_000006.10:g.31084238_31084239del NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-37-2188_-37-2187del NP_001185744.1:n.-37-2188_-37-2187del
NM_001318484.1:c.8-2223_8-2222del NP_001305413.1:n.8-2223_8-2222del