Canonical Allele Identifier: CA1087405634
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs10632347

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008563_31008566dup , CM000668.2:g.31008563_31008566dup GRCh38
NC_000006.11:g.30976340_30976343dup , CM000668.1:g.30976340_30976343dup GRCh37
NC_000006.10:g.31084319_31084322dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2107_-37-2104dup NP_001185744.1:n.-37-2107_-37-2104dup
NM_001318484.1:c.8-2142_8-2139dup NP_001305413.1:n.8-2142_8-2139dup