Canonical Allele Identifier: CA1087405563
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763657199
gnomAD v3: 6-31008534-A-G
gnomAD v4: 6-31008534-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008534A>G , CM000668.2:g.31008534A>G GRCh38
NC_000006.11:g.30976311A>G , CM000668.1:g.30976311A>G GRCh37
NC_000006.10:g.31084290A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-2136A>G NP_001185744.1:n.-37-2136A>G
NM_001318484.1:c.8-2171A>G NP_001305413.1:n.8-2171A>G