Canonical Allele Identifier: CA136813375
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs931698353
gnomAD v3: 6-31008725-A-C
gnomAD v4: 6-31008725-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008725A>C , CM000668.2:g.31008725A>C GRCh38
NC_000006.11:g.30976502A>C , CM000668.1:g.30976502A>C GRCh37
NC_000006.10:g.31084481A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1945A>C NP_001185744.1:n.-37-1945A>C
NM_001318484.1:c.8-1980A>C NP_001305413.1:n.8-1980A>C