Canonical Allele Identifier: CA823869754
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1362308220
gnomAD v3: 6-31008842-T-C
gnomAD v4: 6-31008842-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008842T>C , CM000668.2:g.31008842T>C GRCh38
NC_000006.11:g.30976619T>C , CM000668.1:g.30976619T>C GRCh37
NC_000006.10:g.31084598T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-37-1828T>C NP_001185744.1:n.-37-1828T>C
NM_001318484.1:c.8-1863T>C NP_001305413.1:n.8-1863T>C