Canonical Allele Identifier: CA566327164

Gene: MUC22

Linked Data

• dbSNP Id: rs1193787077
• gnomAD v2: 6-30976360-C-G
• gnomAD v3: 6-31008583-C-G
• gnomAD v4: 6-31008583-C-G
• MyVariant Identifiers: chr6:g.30976360C>G (hg19) ; chr6:g.31008583C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31008583C>G , CM000668.2:g.31008583C>G	GRCh38
NC_000006.11:g.30976360C>G , CM000668.1:g.30976360C>G	GRCh37
NC_000006.10:g.31084339C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001198815.1:c.-37-2087C>G	NP_001185744.1:n.-37-2087C>G
NM_001318484.1:c.8-2122C>G	NP_001305413.1:n.8-2122C>G