Canonical Allele Identifier: CA823869718
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1418637873
gnomAD v3: 6-31008468-A-C
gnomAD v4: 6-31008468-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008468A>C , CM000668.2:g.31008468A>C GRCh38
NC_000006.11:g.30976245A>C , CM000668.1:g.30976245A>C GRCh37
NC_000006.10:g.31084224A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-37-2202A>C NP_001185744.1:n.-37-2202A>C
NM_001318484.1:c.8-2237A>C NP_001305413.1:n.8-2237A>C