Canonical Allele Identifier: CA1087406018
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs117712789
gnomAD v3: 6-31008919-G-C
gnomAD v4: 6-31008919-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008919G>C , CM000668.2:g.31008919G>C GRCh38
NC_000006.11:g.30976696G>C , CM000668.1:g.30976696G>C GRCh37
NC_000006.10:g.31084675G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1751G>C NP_001185744.1:n.-37-1751G>C
NM_001318484.1:c.8-1786G>C NP_001305413.1:n.8-1786G>C