Canonical Allele Identifier: CA823869708

Gene: MUC22

Linked Data

• dbSNP Id: rs138778412
• gnomAD v3: 6-31008293-A-G
• gnomAD v4: 6-31008293-A-G
• MyVariant Identifiers: chr6:g.30976070A>G (hg19) ; chr6:g.31008293A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31008293A>G , CM000668.2:g.31008293A>G	GRCh38
NC_000006.11:g.30976070A>G , CM000668.1:g.30976070A>G	GRCh37
NC_000006.10:g.31084049A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001198815.1:c.-38+2160A>G	NP_001185744.1:n.-38+2160A>G
NM_001318484.1:c.7+2160A>G	NP_001305413.1:n.7+2160A>G