Canonical Allele Identifier: CA136813312
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1008698643
gnomAD v3: 6-31008491-A-C
gnomAD v4: 6-31008491-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008491A>C , CM000668.2:g.31008491A>C GRCh38
NC_000006.11:g.30976268A>C , CM000668.1:g.30976268A>C GRCh37
NC_000006.10:g.31084247A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-37-2179A>C NP_001185744.1:n.-37-2179A>C
NM_001318484.1:c.8-2214A>C NP_001305413.1:n.8-2214A>C