Canonical Allele Identifier: CA823869706
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1355449133

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008255T>A , CM000668.2:g.31008255T>A GRCh38
NC_000006.11:g.30976032T>A , CM000668.1:g.30976032T>A GRCh37
NC_000006.10:g.31084011T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-38+2122T>A NP_001185744.1:n.-38+2122T>A
NM_001318484.1:c.7+2122T>A NP_001305413.1:n.7+2122T>A