Canonical Allele Identifier: CA136813280
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs752630732
gnomAD v3: 6-31008378-C-T
gnomAD v4: 6-31008378-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008378C>T , CM000668.2:g.31008378C>T GRCh38
NC_000006.11:g.30976155C>T , CM000668.1:g.30976155C>T GRCh37
NC_000006.10:g.31084134C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-38+2245C>T NP_001185744.1:n.-38+2245C>T
NM_001318484.1:c.7+2245C>T NP_001305413.1:n.7+2245C>T