Canonical Allele Identifier: CA1087405424
Gene: MUC22 HGNC NCBI

Linked Data

dbSNP Id: rs1763640215
gnomAD v3: 6-31008310-A-G
gnomAD v4: 6-31008310-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31008310A>G , CM000668.2:g.31008310A>G GRCh38
NC_000006.11:g.30976087A>G , CM000668.1:g.30976087A>G GRCh37
NC_000006.10:g.31084066A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001198815.1:c.-38+2177A>G NP_001185744.1:n.-38+2177A>G
NM_001318484.1:c.7+2177A>G NP_001305413.1:n.7+2177A>G