Canonical Allele Identifier: CA1087405529
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763653520
gnomAD v3: 6-31008474-G-C
gnomAD v4: 6-31008474-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008474G>C , CM000668.2:g.31008474G>C GRCh38
NC_000006.11:g.30976251G>C , CM000668.1:g.30976251G>C GRCh37
NC_000006.10:g.31084230G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001198815.1:c.-37-2196G>C NP_001185744.1:n.-37-2196G>C
NM_001318484.1:c.8-2231G>C NP_001305413.1:n.8-2231G>C