Canonical Allele Identifier: CA823869710
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1460978990
gnomAD v3: 6-31008337-C-T
gnomAD v4: 6-31008337-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008337C>T , CM000668.2:g.31008337C>T GRCh38
NC_000006.11:g.30976114C>T , CM000668.1:g.30976114C>T GRCh37
NC_000006.10:g.31084093C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-38+2204C>T NP_001185744.1:n.-38+2204C>T
NM_001318484.1:c.7+2204C>T NP_001305413.1:n.7+2204C>T